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CPC Scientific

Full company profile

uuid0009qi8

Namestring
CPC Scientific
Legal namestring
CPC Scientific Inc.
Company typeenum
Private
Founded yearint
2001
Descriptiontext

CPC Scientific is a Contract Research, Development, and Manufacturing Organization (CRDMO) founded in 2001 and headquartered in Rocklin, California, with primary GMP manufacturing operations in Hangzhou, China, through its Chinese Peptide Company subsidiary. The company is a wholly owned subsidiary of Hong Kong-listed Medtide Inc. (HKEX: 03880), which completed its IPO in June 2025. CPC Scientific specializes in synthetic peptide and oligonucleotide production, with core technical capabilities spanning Solid-Phase Peptide Synthesis (Fmoc, Boc, Cbz), Liquid-Phase Synthesis, ligation chemistry, and peptide-oligonucleotide conjugates including POCs, PDCs, and RDCs. It maintains 26,000 sqm of GMP manufacturing infrastructure with 19 synthesis suites, 16 purification suites, reactor volumes up to 1,000L, and an annual API capacity exceeding 1,000 kg at 20-25 kg per batch.

The company's product and service portfolio spans the full peptide lifecycle: custom research-grade peptide synthesis, a 1,200+ sequence catalog across 21 research areas, FTE-based discovery services, GMP peptide manufacturing for Phase I through commercial supply, GMP oligonucleotide manufacturing (1-17 kg annual capacity), generic peptide API development (Leuprorelin, Triptorelin, Cetrorelix, Goserelin, Teduglutide), cosmetic peptides, neoantigen peptides, and a broad peptide modifications portfolio (macrocycles, stapled peptides, PEGylated, dye-labeled, glycosylated, click, peptoids, long sequences, D-amino acids, isotope-labeled). Regulatory credentials include FDA DMFs for Tirzepatide (DMF 043979, May 2026) and Cetrorelix (DMF 034884), five successful FDA inspections, and certifications from EMA, TGA, MFDS, NMPA, and three ISO standards.

CPC Scientific operates an enterprise field-sales model supplemented by industry conference presence (CPHI Frankfurt/Korea/Milan, TIDES Europe, BioJapan, DCAT), direct quotation-based GMP sales, an e-commerce catalog for research peptides, and FedEx international shipping across 50+ countries. Customer segments span pharmaceutical companies, biotechnology companies, academic and research institutions, cosmetics companies, and generic drug manufacturers, with 300+ ongoing CMC development projects and 13 commercial GMP programs as of 2025. Revenue is generated through one-time custom and catalog purchases, multi-year managed GMP manufacturing contracts, FTE-based professional services, and commercial API licensing, though specific revenue figures are not publicly disclosed.

Short descriptiontext

CPC Scientific is a CRDMO specializing in synthetic peptides and oligonucleotides, serving pharmaceutical, biotechnology, academic, cosmetic, and generic drug manufacturers globally through custom research, GMP manufacturing, and commercial API production across 50+ countries.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersRocklin, United States
HQ citystring
Rocklin
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
peptide CDMO services, oligonucleotide manufacturing, GMP peptide API, custom peptide synthesis, peptide oligonucleotide conjugates
Industry3 codes
1CMC & Pharmaceutical Development (Formulation/Process/Analytical Development)
CodeHLAIALADPrimaryYes
2Regulatory Strategy & Global Submissions (IND/CTA/NDA/BLA/MAA)
CodeHLAGAKAAPrimaryNo
3Central Laboratory & Clinical Trial Testing CROs
CodeHLAGAAAEPrimaryNo
NAICS code3 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical and Medicine Manufacturing3254
SIC code2 codes
  • Services-Commercial Physical & Biological Research8731
  • Pharmaceutical Preparations2834
Product category
Contract Peptide and Oligonucleotide Manufacturing (CRDMO)
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model6 records
1Custom Peptide Synthesis Services
TypeOne Time License
Description

CRO services including peptide NCE discovery synthesis and custom peptide manufacturing for research purposes

cpcscientific.com
2GMP Peptide Manufacturing (CDMO)
TypeManaged Services
Description

Contract development and manufacturing services for peptide CMC development, late-phase development, and commercial production under GMP conditions

cpcscientific.com
3Commercial API Manufacturing (CMO)
TypeOne Time License
Description

Contract manufacturing for peptide NCE and generic drug commercial production, including regulatory filing support (DMF preparation)

cpcscientific.com
4Catalog Peptide Sales
TypeOne Time License
Description

Sale of pre-made catalog peptides (1,200+ sequences across 21 research areas) with pricing from $16.50 to $1,386+ per unit

cpcscientific.com
5FTE (Full-Time Equivalent) Services
TypeProfessional Services
Description

Discovery chemistry services providing dedicated scientific staff allocation for flexible, continuous project support

cpcscientific.com
6Generic Peptide APIs
TypeOne Time License
Description

Commercial generic peptide API manufacturing for approved indications including cancer, diabetes, obesity, and multiple sclerosis treatments

cpcscientific.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Personnel, Operations, Supply Chain, Infrastructure, Technology or R&D, Marketing or Sales
Pricing details3 tiers
1Catalog peptides available in various sizes (mg to multi-mg)
ModelUnit PricingBilling cadencePay-as-you-go
Notes

Charybdotoxin: $172.70–$1,298.00; Vasopressin: $27.50; Angiotensin I/II: $22.00–$654.50; DJK-5: $70.00–$1,199.00; Most catalog peptides 95% pure TFA salts

cpcscientific.com
2FTE Model for discovery chemistry services
ModelOtherBilling cadenceMulti-year contract
Notes

Flexible resource allocation with dedicated scientific support; continuous project engagement; cost efficiency through FTE-based pricing model

cpcscientific.com
3GMP Manufacturing Services
ModelOtherBilling cadenceMulti-year contract
Notes

Phase-appropriate control systems; CMC development for IND/NDA; DMF compilation and submission; Quote-based pricing for custom projects

cpcscientific.com
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

CPC Scientific is a Contract Research, Development, and Manufacturing Organization (CRDMO) that provides end-to-end synthetic peptide and oligonucleotide services to pharmaceutical and biotechnology companies. Its core offerings span custom research peptide synthesis and catalog peptide sales, peptide modifications (macrocycles, stapled peptides, PEGylation, glycosylation, etc.), Phase I–III and commercial GMP peptide manufacturing, generic peptide API production, GMP oligonucleotide manufacturing, and integrated peptide-oligonucleotide conjugates (POC/PDC/RDC).

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • 300+ ongoing CMC development projects supported
+4 more records
Product overview1 text field

CPC Scientific is a Contract Research, Development, and Manufacturing Organization (CRDMO) specializing in synthetic peptides and oligonucleotides. The company operates as a single integrated platform offering end-to-end services from discovery through commercial manufacturing. The core product portfolio centers on GMP Peptide Manufacturing (including Phase I-III and commercial GMP programs), Research Peptides (custom synthesis and catalog offerings with 1,200+ sequences), and GMP Oligonucleotide Manufacturing. These are supplemented by Peptide-Oligonucleotide Conjugates, Generic Peptides API Development, Cosmetic Peptides, Neoantigen Peptides, FTE Services, and a comprehensive Peptide Modifications Portfolio covering macrocycles, stapled peptides, PEGylation, dye-labeling, and other specialized modifications. The platform is vertically integrated to support pharmaceutical and biotech partners across the entire therapeutic lifecycle.

Product and service8 records
1GMP Peptide Manufacturing
CategoryGMP peptide manufacturing
Description

Large-scale, late-phase, and commercial GMP peptide manufacturing services with annual API production capacity over 1,000 kg and per-batch capacity of 20–25 kg. Supports projects from early discovery through commercialization with CGMP compliance for NMPA, FDA, EMA, TGA, and MFDS regulatory authorities. For pharmaceutical and biotechnology clients.

2Custom Peptide Synthesis (Research Peptides)
CategoryCustom peptide synthesis
Description

Custom peptide synthesis services providing reliable, high-quality peptides directly to researchers and institutions, including complex modifications (macrocycles, stapled peptides, dye-labeled, PEGylated, click, glycosylated, phosphorylated, peptoids, unnatural amino acids, peptide libraries, lipopeptides, multiple disulfide bridges, long sequences, D-amino acids, isotope labeled). Includes a 1,200+ catalog of pre-made peptides across 21 research areas.

3GMP Oligonucleotide Manufacturing
CategoryOligonucleotide manufacturing
Description

Research-grade and clinical-grade oligonucleotide manufacturing services spanning from discovery to clinical phases, with recently reconfigured capacity for 1–17 kilograms of oligonucleotides annually.

4Peptide-Oligonucleotide Conjugates
CategoryPeptide-oligonucleotide conjugates
Description

Seamlessly integrates peptide and oligonucleotide platforms to produce peptide conjugates including peptide-oligonucleotide conjugates (POC), peptide drug conjugates (PDC), and radionuclide drug conjugates (RDC).

5Generic Peptide API Development
CategoryGeneric peptide API
Description

Commercial generic API manufacturing including Leuprorelin Acetate, Triptorelin Acetate, Cetrorelix Acetate, Goserelin Acetate, Triptorelin Pamoate, and Teduglutide for treatment of cancer, diabetes, obesity, and multiple sclerosis.

6Cosmetic Peptides
CategoryCosmetic peptide manufacturing
Description

Cosmetic peptide ingredient synthesis for anti-aging, wound healing, and skin care applications. Manufacturing capacity ranges from mg quantities through 100 kg commercialization scale, with ISO 22716 GMP compliance.

7Neoantigen Peptides
CategoryNeoantigen peptide synthesis
Description

Custom neoantigen peptide synthesis services for personalized therapeutic applications.

8FTE Services
CategoryDiscovery chemistry services
Description

Full-time equivalent (FTE) based discovery chemistry services for synthetic peptides, providing dedicated scientific support with flexible resource allocation and continuous project engagement.

Scale indicator12 records

Each record includes

Type, Value, Description, Source

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Global CDMO with a dedicated peptide platform offering custom synthesis, GMP manufacturing, and generic peptide APIs across multiple sites—competes head-to-head with CPC for both commercial peptide API and complex modification projects.

TypeBroad incumbent
Description

Largest global CDMO with a peptide and small-molecule API platform alongside biologics, cell & gene, and other modalities—overlaps with CPC on peptide CMC and commercial API but operates at far greater scale and modality breadth.

TypeEmerging player
Description

India-based integrated CRDMO with peptide, small molecule, and biologics capabilities—competes with CPC for biotech CDMO contracts, particularly for customers seeking alternative geographic supply outside US/EU/China.

TypeDirect peer
Description

China-based CRDMO with a major peptide and oligonucleotide franchise plus much broader small molecule and biologic capabilities—directly comparable to CPC's peptide CRDMO model while also competing on geographic flexibility and scale.

TypeDirect peer
Description

Public peptide CDMO offering custom and GMP-grade peptides for pharma and biotech, with comparable end-to-end capabilities across APIs, generic peptides, and complex modifications—directly competes with CPC for the same customer profile.

TypeDirect peer
Description

Swiss peptide CDMO offering custom peptide synthesis, GMP production, and a generic peptide API portfolio—directly comparable to CPC's discovery-through-commercial peptide services for pharma and biotech customers.

TypeDirect peer
Description

Swiss-headquartered global leader in peptide and oligonucleotide CDMO services with large-scale GMP manufacturing, extensive DMF portfolio, and a similar end-to-end offering from custom synthesis through commercial API production—CPC's most direct competitor in peptide API.

TypeEmerging player
Description

CDMO arm of GenScript offering peptide synthesis, biologics, plasmid, and cell therapy services with growing GMP capacity—an emerging player whose peptide services increasingly compete with CPC for biotech customers in Asia and globally.

TypeDirect peer
Description

Specialist oligonucleotide CDMO offering custom and GMP oligo manufacturing—directly comparable to CPC's recently expanded GMP oligonucleotide platform and peptide-oligonucleotide conjugate capability.

TypeDirect peer
Description

US- and China-based peptide CDMO specializing in custom peptide synthesis, GMP manufacturing, and generic peptide APIs—closely comparable to CPC across both research and commercial peptide manufacturing.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment5 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile5 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature7 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles5 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
Compliance8 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

CPC Scientific

Contract Peptide and Oligonucleotide Manufacturing (CRDMO)cpcscientific.com

CPC Scientific is a CRDMO specializing in synthetic peptides and oligonucleotides, serving pharmaceutical, biotechnology, academic, cosmetic, and generic drug manufacturers globally through custom research, GMP manufacturing, and commercial API production across 50+ countries.

What CPC Scientific does

CPC Scientific is a Contract Research, Development, and Manufacturing Organization (CRDMO) founded in 2001 and headquartered in Rocklin, California, with primary GMP manufacturing operations in Hangzhou, China, through its Chinese Peptide Company subsidiary. The company is a wholly owned subsidiary of Hong Kong-listed Medtide Inc. (HKEX: 03880), which completed its IPO in June 2025. CPC Scientific specializes in synthetic peptide and oligonucleotide production, with core technical capabilities spanning Solid-Phase Peptide Synthesis (Fmoc, Boc, Cbz), Liquid-Phase Synthesis, ligation chemistry, and peptide-oligonucleotide conjugates including POCs, PDCs, and RDCs. It maintains 26,000 sqm of GMP manufacturing infrastructure with 19 synthesis suites, 16 purification suites, reactor volumes up to 1,000L, and an annual API capacity exceeding 1,000 kg at 20-25 kg per batch.

The company's product and service portfolio spans the full peptide lifecycle: custom research-grade peptide synthesis, a 1,200+ sequence catalog across 21 research areas, FTE-based discovery services, GMP peptide manufacturing for Phase I through commercial supply, GMP oligonucleotide manufacturing (1-17 kg annual capacity), generic peptide API development (Leuprorelin, Triptorelin, Cetrorelix, Goserelin, Teduglutide), cosmetic peptides, neoantigen peptides, and a broad peptide modifications portfolio (macrocycles, stapled peptides, PEGylated, dye-labeled, glycosylated, click, peptoids, long sequences, D-amino acids, isotope-labeled). Regulatory credentials include FDA DMFs for Tirzepatide (DMF 043979, May 2026) and Cetrorelix (DMF 034884), five successful FDA inspections, and certifications from EMA, TGA, MFDS, NMPA, and three ISO standards.

CPC Scientific operates an enterprise field-sales model supplemented by industry conference presence (CPHI Frankfurt/Korea/Milan, TIDES Europe, BioJapan, DCAT), direct quotation-based GMP sales, an e-commerce catalog for research peptides, and FedEx international shipping across 50+ countries. Customer segments span pharmaceutical companies, biotechnology companies, academic and research institutions, cosmetics companies, and generic drug manufacturers, with 300+ ongoing CMC development projects and 13 commercial GMP programs as of 2025. Revenue is generated through one-time custom and catalog purchases, multi-year managed GMP manufacturing contracts, FTE-based professional services, and commercial API licensing, though specific revenue figures are not publicly disclosed.

CPC Scientific firmographics

Firmographics
Name
CPC Scientific
Legal name
CPC Scientific Inc.
Website
https://cpcscientific.com
Company type
Private
Founded year
2001
Operating status
Operating
Headcount range
501–1,000 employees
Short description
CPC Scientific is a CRDMO specializing in synthetic peptides and oligonucleotides, serving pharmaceutical, biotechnology, academic, cosmetic, and generic drug manufacturers globally through custom research, GMP manufacturing, and commercial API production across 50+ countries.
Ownership category
akta.pro rank

CPC Scientific industry classification

Industry
Product category
Contract Peptide and Oligonucleotide Manufacturing (CRDMO)
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical and Medicine Manufacturing (3254)
SIC
Services-Commercial Physical & Biological Research (8731), Pharmaceutical Preparations (2834)
akta.pro primary industry
CMC & Pharmaceutical Development (Formulation/Process/Analytical Development) (HLAIALAD)
akta.pro secondary industries
Regulatory Strategy & Global Submissions (IND/CTA/NDA/BLA/MAA) (HLAGAKAA), Central Laboratory & Clinical Trial Testing CROs (HLAGAAAE)

Keywords

  • Peptide CDMO services
  • Oligonucleotide manufacturing
  • GMP peptide API
  • Custom peptide synthesis
  • Peptide oligonucleotide conjugates

Where CPC Scientific is headquartered

Location

Headquarters

HQ city
Rocklin
HQ country
United States
HQ region
North America

Offices3 records

Markets served

CPC Scientific business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Supply Chain, Infrastructure, Technology or R&D, Marketing or Sales

Revenue model

  1. Custom Peptide Synthesis Services: CRO services including peptide NCE discovery synthesis and custom peptide manufacturing for research purposes
  2. GMP Peptide Manufacturing (CDMO): Contract development and manufacturing services for peptide CMC development, late-phase development, and commercial production under GMP conditions
  3. Commercial API Manufacturing (CMO): Contract manufacturing for peptide NCE and generic drug commercial production, including regulatory filing support (DMF preparation)
  4. Catalog Peptide Sales: Sale of pre-made catalog peptides (1,200+ sequences across 21 research areas) with pricing from $16.50 to $1,386+ per unit
  5. FTE (Full-Time Equivalent) Services: Discovery chemistry services providing dedicated scientific staff allocation for flexible, continuous project support
  6. Generic Peptide APIs: Commercial generic peptide API manufacturing for approved indications including cancer, diabetes, obesity, and multiple sclerosis treatments

Pricing tiers

ModelBillingPrice
Unit PricingPay-as-you-goCatalog peptides available in various sizes (mg to multi-mg)
OtherMulti-year contractFTE Model for discovery chemistry services
OtherMulti-year contractGMP Manufacturing Services

Go-to-market motion2 records

Distribution channels4 records

Marketing channels6 records

CPC Scientific product offering

Product offering

Core offering

CPC Scientific is a Contract Research, Development, and Manufacturing Organization (CRDMO) that provides end-to-end synthetic peptide and oligonucleotide services to pharmaceutical and biotechnology companies. Its core offerings span custom research peptide synthesis and catalog peptide sales, peptide modifications (macrocycles, stapled peptides, PEGylation, glycosylation, etc.), Phase I–III and commercial GMP peptide manufacturing, generic peptide API production, GMP oligonucleotide manufacturing, and integrated peptide-oligonucleotide conjugates (POC/PDC/RDC).

Product overview

CPC Scientific is a Contract Research, Development, and Manufacturing Organization (CRDMO) specializing in synthetic peptides and oligonucleotides. The company operates as a single integrated platform offering end-to-end services from discovery through commercial manufacturing. The core product portfolio centers on GMP Peptide Manufacturing (including Phase I-III and commercial GMP programs), Research Peptides (custom synthesis and catalog offerings with 1,200+ sequences), and GMP Oligonucleotide Manufacturing. These are supplemented by Peptide-Oligonucleotide Conjugates, Generic Peptides API Development, Cosmetic Peptides, Neoantigen Peptides, FTE Services, and a comprehensive Peptide Modifications Portfolio covering macrocycles, stapled peptides, PEGylation, dye-labeling, and other specialized modifications. The platform is vertically integrated to support pharmaceutical and biotech partners across the entire therapeutic lifecycle.

Differentiator

Problem solved

Functional benefit

Products and services

  • GMP Peptide Manufacturing Large-scale, late-phase, and commercial GMP peptide manufacturing services with annual API production capacity over 1,000 kg and per-batch capacity of 20–25 kg. Supports projects from early discovery through commercialization with CGMP compliance for NMPA, FDA, EMA, TGA, and MFDS regulatory authorities. For pharmaceutical and biotechnology clients.
  • Custom Peptide Synthesis (Research Peptides) Custom peptide synthesis services providing reliable, high-quality peptides directly to researchers and institutions, including complex modifications (macrocycles, stapled peptides, dye-labeled, PEGylated, click, glycosylated, phosphorylated, peptoids, unnatural amino acids, peptide libraries, lipopeptides, multiple disulfide bridges, long sequences, D-amino acids, isotope labeled). Includes a 1,200+ catalog of pre-made peptides across 21 research areas.
  • GMP Oligonucleotide Manufacturing Research-grade and clinical-grade oligonucleotide manufacturing services spanning from discovery to clinical phases, with recently reconfigured capacity for 1–17 kilograms of oligonucleotides annually.
  • Peptide-Oligonucleotide Conjugates Seamlessly integrates peptide and oligonucleotide platforms to produce peptide conjugates including peptide-oligonucleotide conjugates (POC), peptide drug conjugates (PDC), and radionuclide drug conjugates (RDC).
  • Generic Peptide API Development Commercial generic API manufacturing including Leuprorelin Acetate, Triptorelin Acetate, Cetrorelix Acetate, Goserelin Acetate, Triptorelin Pamoate, and Teduglutide for treatment of cancer, diabetes, obesity, and multiple sclerosis.
  • Cosmetic Peptides Cosmetic peptide ingredient synthesis for anti-aging, wound healing, and skin care applications. Manufacturing capacity ranges from mg quantities through 100 kg commercialization scale, with ISO 22716 GMP compliance.
  • Neoantigen Peptides Custom neoantigen peptide synthesis services for personalized therapeutic applications.
  • FTE Services Full-time equivalent (FTE) based discovery chemistry services for synthetic peptides, providing dedicated scientific support with flexible resource allocation and continuous project engagement.

Quantifiable outcome

  • 300+ ongoing CMC development projects supported
  • +4 more outcomes

Companies that use CPC Scientific

Customer profile

Named customers3 records

Segments5 records

Ideal customer profiles5 records

CPC Scientific technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature7 records

CPC Scientific partnerships and signals

Strategic signal

Scale indicators12 records

Recent moves7 records

Expansion highlights5 records

CPC Scientific competitors and assessment

Company assessment

Direct peers

  • CordenPharma: Global CDMO with a dedicated peptide platform offering custom synthesis, GMP manufacturing, and generic peptide APIs across multiple sites—competes head-to-head with CPC for both commercial peptide API and complex modification projects.
  • WuXi STA (WuXi AppTec): China-based CRDMO with a major peptide and oligonucleotide franchise plus much broader small molecule and biologic capabilities—directly comparable to CPC's peptide CRDMO model while also competing on geographic flexibility and scale.
  • PolyPeptide Group: Public peptide CDMO offering custom and GMP-grade peptides for pharma and biotech, with comparable end-to-end capabilities across APIs, generic peptides, and complex modifications—directly competes with CPC for the same customer profile.
  • Senn Chemicals: Swiss peptide CDMO offering custom peptide synthesis, GMP production, and a generic peptide API portfolio—directly comparable to CPC's discovery-through-commercial peptide services for pharma and biotech customers.
  • Bachem: Swiss-headquartered global leader in peptide and oligonucleotide CDMO services with large-scale GMP manufacturing, extensive DMF portfolio, and a similar end-to-end offering from custom synthesis through commercial API production—CPC's most direct competitor in peptide API.
  • Avecia (Nitto Denko Avecia): Specialist oligonucleotide CDMO offering custom and GMP oligo manufacturing—directly comparable to CPC's recently expanded GMP oligonucleotide platform and peptide-oligonucleotide conjugate capability.
  • AmbioPharm: US- and China-based peptide CDMO specializing in custom peptide synthesis, GMP manufacturing, and generic peptide APIs—closely comparable to CPC across both research and commercial peptide manufacturing.

Broad incumbents

  • Lonza: Largest global CDMO with a peptide and small-molecule API platform alongside biologics, cell & gene, and other modalities—overlaps with CPC on peptide CMC and commercial API but operates at far greater scale and modality breadth.

Emerging players

  • Syngene International: India-based integrated CRDMO with peptide, small molecule, and biologics capabilities—competes with CPC for biotech CDMO contracts, particularly for customers seeking alternative geographic supply outside US/EU/China.
  • GenScript ProBio: CDMO arm of GenScript offering peptide synthesis, biologics, plasmid, and cell therapy services with growing GMP capacity—an emerging player whose peptide services increasingly compete with CPC for biotech customers in Asia and globally.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

CPC Scientific social profiles

Digital presence

CPC Scientific compliance and trust

Trust signal

Compliance8 records

CPC Scientific financial estimates

Financial estimate

Revenue estimate

Valuation estimate

CPC Scientific leadership team

Management profile

Number of profiles

Profiles5 records

CPC Scientific funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

CPC Scientific M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about CPC Scientific

What does CPC Scientific do?

CPC Scientific is a Contract Research, Development, and Manufacturing Organization (CRDMO) that provides end-to-end synthetic peptide and oligonucleotide services to pharmaceutical and biotechnology companies. Its core offerings span custom research peptide synthesis and catalog peptide sales, peptide modifications (macrocycles, stapled peptides, PEGylation, glycosylation, etc.), Phase I–III and commercial GMP peptide manufacturing, generic peptide API production, GMP oligonucleotide manufacturing, and integrated peptide-oligonucleotide conjugates (POC/PDC/RDC).

Is CPC Scientific a public or private company?

CPC Scientific is a private company. It is classified as corporate owned and is currently operating.

When was CPC Scientific founded?

CPC Scientific was founded in 2001. It employs 501 to 1,000 people.

Where is CPC Scientific based?

CPC Scientific is headquartered in Rocklin, United States, in the North America region.

How does CPC Scientific make money?

Six revenue lines are on record. Custom Peptide Synthesis Services are the primary driver. The others are GMP Peptide Manufacturing (CDMO), commercial API Manufacturing (CMO), catalog Peptide Sales, FTE (Full-Time Equivalent) Services and generic Peptide APIs.

Who are CPC Scientific's main competitors?

Direct peers on record are CordenPharma, WuXi STA (WuXi AppTec), PolyPeptide Group, Senn Chemicals, Bachem, Avecia (Nitto Denko Avecia) and AmbioPharm. Lonza is listed as a broad incumbent. Emerging players are Syngene International and GenScript ProBio.

Does CPC Scientific have an API?

No public API is recorded for CPC Scientific.

What industry is CPC Scientific in?

CPC Scientific's product category is Contract Peptide and Oligonucleotide Manufacturing (CRDMO). Its primary akta.pro industry code is HLAIALAD, CMC & Pharmaceutical Development (Formulation/Process/Analytical Development), with a secondary code of HLAGAKAA, Regulatory Strategy & Global Submissions (IND/CTA/NDA/BLA/MAA). Its NAICS code is 541714 and its SIC code is 8731.

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Live signals
Business Wire BlogCPC Scientific Announces U.S. FDA Pre-License Inspection (PLI) Successfully Completed at Its Hangzhou cGMP Manufacturing Facility for Hepcludex® API, Establishing a Proven Track Record Under the StrinCPC Scientific announced the successful completion of a U.S. FDA Pre-License Inspection at its Hangzhou manufacturing facility for Hepcludex® API, which received accelerated approval for treating chronic hepatitis delta virus (HDV). The inspection evaluated the facility's manufacturing process for a long-chain peptide API that is classified as a biologic under FDA regulations.FinancialContent Business PageCPC Scientific Announces U.S. FDA Pre-License Inspection (PLI) Successfully Completed at Its Hangzhou cGMP Manufacturing Facility for Hepcludex® API, Establishing a Proven Track Record Under the StrinCPC Scientific Inc., a subsidiary of Medtide Inc., announced the successful completion of a FDA Pre-License Inspection at its Hangzhou manufacturing facility for Hepcludex® API, which received FDA approval in May 2026 for treating chronic hepatitis delta virus (HDV) in the U.S. The inspection evaluated the facility's manufacturing of a synthetic long-chain peptide API, addressing a critical unmet medical need.PharmiWeb.comCPC Scientific to Showcase Peptide and Oligonucleotide CDMO Leadership at CPHI Frankfurt 2025CPC Scientific Inc., a peptide and oligonucleotide CDMO and subsidiary of Medtide Inc., will showcase its CRDMO leadership at CPHI Frankfurt 2025 from October 28–30 at Messe Frankfurt, Germany. The company reports nearly 25 years of expertise with a >99.95% new-molecule synthesis success rate, having passed 5 FDA GMP inspections and 3 additional inspections by EMA, MFDS, and TGA, plus 9 NMPA inspections in the past five years. CPC Scientific expects multiple pipeline projects to enter commercial production in the next three to five years, driven by rising global demand for peptide drugs, especially GLP-1 and obesity products.CpcscientificHow Our FTE Model Enables Flexible, Cost-Efficient Peptide Manufacturing SupportThis is not a news article but rather a corporate marketing/service description page from CPC Scientific detailing their Full-Time Equivalent (FTE) model for peptide manufacturing support. The page explains how their FTE services provide dedicated scientific teams, flexible resource allocation, and cost-efficient collaboration for pharmaceutical and biotech clients engaged in peptide development programs. There is no reported news event, breaking development, or current happening — the content serves as promotional material describing CPC Scientific's service offerings and capabilities.CpcscientificWhat is a CDMO, and How Does Partnering With One Accelerate Your Programs?CPC Scientific promotes its capabilities as a Contract Development and Manufacturing Organization (CDMO) specializing in peptide and oligonucleotide therapies, highlighting its global GMP manufacturing infrastructure. The company is expanding its capacity with a new facility in Rocklin, California, scheduled to open in 2026, to support the growing market demand for GLP-1 therapies and other pipeline projects.CpcscientificPEGylated PeptidesThe article outlines the technical challenges of using peptides in pharmaceuticals, such as rapid degradation and poor solubility, and describes PEGylation as a method to enhance therapeutic efficacy by reducing immunogenicity and renal clearance. It details specific chemical methodologies for site-specific PEGylation, including Click Chemistry and Suzuki-Miyaura Coupling, which are critical for achieving monodispersed conjugates required for FDA approval. CPC Scientific is identified as a provider capable of performing these specialized site-specific PEGylation services.PR NewswireCPC Scientific Announces New California Peptide API Manufacturing FacilityCPC Scientific Inc., a global peptide CRDMO, has invested in a new 41,000 sq ft manufacturing facility in Rocklin, California to produce clinical to commercial-grade peptide Active Pharmaceutical Ingredients, bringing new life-science manufacturing jobs to the area. The facility, scheduled to be operational by 2023, will expand the company's North American manufacturing footprint and diversify its supply chain, complementing its existing operations in Hangzhou, China. The expansion aims to meet growing worldwide demand for peptide-based therapeutics, which have been the fastest-growing sector among chemically synthesized new drug candidates.CpcscientificWhy solid-phase synthesis?The article presents a collection of technical white papers and case studies from CPC Scientific regarding innovations in solid-phase peptide synthesis (SPPS). These documents detail methods for sustainable large-scale production, green synthesis strategies, and the development of specialized therapeutic peptides such as stapled peptides and those used in radionuclide therapy. The content highlights process improvements aimed at enhancing efficiency, atom economy, and drug efficacy while minimizing environmental impact.PR NewswireCPC Scientific Successfully Passes 4th U.S. FDA InspectionCPC Scientific announced that its Good Manufacturing Practice facility in Hangzhou, China has successfully passed its fourth U.S. FDA inspection, with no Form 483 observations issued. This marks the latest milestone in the company's regulatory compliance record, with executives citing adherence to standards across Europe, China, Japan, ICH, and WHO. The company stated the results demonstrate its commitment to quality and its ability to support future global peptide market growth through planned facility expansion.