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Dor Pharmaceutical Services

Full company profile

uuid000ksp8

Namestring
Dor Pharmaceutical Services
Legal namestring
Novolog (Pharm Up 1966) Ltd.
Websiteurl
dor-ps.com
Company typeenum
Private
Founded yearint
2011
Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersModi'in, Israel
HQ citystring
Modi'in
HQ countrystring
Israel
HQ regionstring
Middle East
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
pharmaceutical regulatory services, quality assurance consulting, medical device compliance, pharmacovigilance services, clinical trial coordination
Industry2 codes
1Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC)
CodeHLAGAHAMPrimaryYes
2Manufacturing, MSAT & Operations Staffing (API/Biologics/Cell & Gene)
CodeHLAGAOALPrimaryNo
NAICS code3 codes
  • Professional, Scientific, and Technical Services54
  • Scientific Research and Development Services5417
  • Management Consulting Services54161
SIC code2 codes
  • Services-Health Services8000
  • Services-Commercial Physical & Biological Research8731
Product category
Pharmaceutical Regulatory Services
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model5 records
1Regulatory Affairs and Registration Services
TypeProfessional Services
Description

On-demand regulatory affairs outsourcing, including new drug registration, registration maintenance, appointed pharmacist services, and Marketing Authorization Holder (MAH) services for pharmaceutical, medical device, medical cannabis, cosmetics, and food supplement companies in Israel.

dor-ps.com
2QP and QA Services
TypeProfessional Services
Description

Qualified Person (QP) certification, batch release services, and ongoing quality assurance management to help companies comply with GMP guidelines and Israeli Ministry of Health regulations.

dor-ps.com
3Labeling, Translation, and Printing Services
TypeProfessional Services
Description

End-to-end product labeling and localization, including translation, graphic design, proofreading, and printing of packaging materials (leaflets, labels, folding cartons) for pharmaceutical, medical device, cosmetics, and food supplement products.

dor-ps.com
4Pharmacovigilance and Medical Information Services
TypeProfessional Services
Description

Provided through sister company Medicalix, covering adverse event reporting, device vigilance, medical information, contact center services, and QPPV services for both marketed and clinical trial products.

dor-ps.com
5Clinical Trial Services
TypeProfessional Services
Description

Full outsourcing of clinical trial coordination at leading Israeli medical centers, including protocol translation, informed consent form translation, regulatory submissions, and supply chain management.

dor-ps.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components5 values
Personnel, Operations, Technology or R&D, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 record
1Medicalix
Description

A sister company of Dor Pharmaceutical Services specializing in pharmacovigilance, device vigilance, and medical information services.

Core offering1 text field

Dor Pharmaceutical Services is an Israeli B2B regulatory and quality services provider that supports pharmaceutical, medical device, medical cannabis, cosmetics, and food supplement companies with new drug registration, registration maintenance, Qualified Person (QP) and Quality Assurance (QA) services, GMP-certified labeling/translation/printing, pharmacovigilance, and clinical trial coordination. The company operates an outsourced regulatory affairs department model that extends or fully replaces client regulatory and QA teams on a flexible, on-demand basis, and serves as a one-stop-shop for navigating Israeli Ministry of Health requirements.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • Successfully accompanied IMC-GMP audits under new regulations for medical cannabis companies
+1 more record
Product overview1 text field

Dor Pharmaceutical Services is a comprehensive regulatory and quality services company offering a unified platform of pharmaceutical services. The core offerings include Regulatory Affairs and Drug Registration, Qualified Person (QP) and Quality Assurance (QA) Services, Labeling/Translation/Localization with an in-house GMP printing plant, Clinical Trials Services, and Pharmacovigilance Services. The company operates across five industry verticals: Pharmaceuticals, Medical Devices (AMAR), Food Supplements, Cosmetics, and Medical Cannabis. Services range from new product registration and quality compliance to labeling production and clinical trial coordination. The company is part of Novolog Group's logistics division and serves over 300 customers since its founding in 2011.

Product and service10 records
1Regulatory Affairs and Drug Registration
CategoryRegulatory Affairs
Description

Comprehensive regulatory services for obtaining marketing authorization for pharmaceutical products in Israel, including new drug registration, dossier examination, regulatory compliance, and registration maintenance for both innovative and generic drug manufacturers.

2Qualified Person (QP) and Quality Assurance (QA) Services
CategoryQuality Assurance
Description

Certified QP batch release and QA services helping companies meet GMP guidelines and Israeli Ministry of Health regulations, including batch release, quality system establishment, GMP/GDP audit support, and ongoing quality management.

3Labeling, Translation and Localization Services
CategoryLabeling and Translation
Description

End-to-end product labeling and localization including translation into Hebrew, English, Arabic, and Russian, graphic design, proofreading via Global Vision technology, and printing of packaging materials (leaflets, labels, folding cartons) at the GMP-certified printing plant.

4Clinical Trials Services
CategoryClinical Trials
Description

Full outsourcing services for coordinating clinical trials at leading Israeli medical centers, including protocol translation, informed consent form preparation, regulatory submissions, and supply chain management.

5Pharmacovigilance Services
CategoryPharmacovigilance
Description

Adverse event reporting and monitoring services for pharmaceutical products and medical devices, including device vigilance, medical information, contact center services, and QPPV services for both marketed and clinical trial products, delivered through sister company Medicalix.

6Medical Cannabis Regulatory Services
CategoryMedical Cannabis Compliance
Description

Specialized regulatory services for Israeli medical cannabis companies covering facility establishment, validations, IMC-GMP certification, pharmacy services, product registrations, packaging materials, quality assurance, and clinical research for cultivation, production, distribution, and pharmacy operators.

7Cosmetics Regulatory Services
CategoryCosmetics Regulatory
Description

Regulatory affairs support for cosmetics in Israel, including product registration, labeling compliance, safety assessments, Product Information File (PIF) management, and support for adapting to the new Israeli Ministry of Health cosmetics directive and EC Regulation No 1223/2009.

8Food Supplements Regulatory Services
CategoryFood Supplement Regulatory
Description

Comprehensive regulatory solutions for food supplement manufacturers, importers, and distributors to obtain product regulatory approval in Israel, covering dietary supplements, vitamins, nutritional supplements, herbal products, and homeopathic remedies.

9Medical Devices Regulatory Services
CategoryMedical Device Regulatory
Description

Focused regulatory solutions for medical device companies covering Israeli and international requirements, including AMAR (Medical Device Registration) with Israeli Ministry of Health, ISO 13485 compliance, device classification, import/export regulatory affairs, and quality management system support across all device classes.

10GMP Printing and Relabeling Facility
CategoryPrinting and Packaging
Description

GMP-certified printing facility providing healthcare product labeling, including relabeling services and offset and digital printing on various substrates under cGMP, Israeli Ministry of Health, and multinational pharma company guidelines, managed by a qualified pharmacist and controlled by quality bodies.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
Strategic tierCoreTypeOthers
Description

Dor is part of the Logistics Division of Novolog Group (TASE: NVLG), a senior strategic logistics partner of global pharma companies operating in Israel. Novolog Group employs more than 800 people and provides healthcare logistics, import, and distribution of medicines and medical devices, home healthcare and personalized healthcare, and medical information digital services.

Strategic tierCoreTypeTechnology or Integration
Description

Medicalix is Dor's sister company and the leading pharmacovigilance service provider in Israel. Dor outsources its pharmacovigilance (PV), device vigilance, and medical information (MI) services through Medicalix, enabling companies to comply with applicable local regulations for both marketed and clinical trial products.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
1Regintel Consulting
TypeEmerging player
Description

Regintel is a smaller regulatory affairs consultancy serving pharma and consumer health companies. Comparable to Dor's regulatory service offering but with narrower geographic and therapeutic reach.

TypeDirect peer
Description

Arriello is a regulatory affairs, pharmacovigilance, and quality/compliance consultancy for pharma, biotech, and medical device companies across Europe and Israel. Closely comparable to Dor in service mix (RA, QP/QA, PV, labeling) and customer profile, with similar geographic focus.

TypeDirect peer
Description

The Weinberg Group is a regulatory and quality compliance consulting firm serving pharma, biotech, and medical device clients. Directly comparable to Dor on regulatory affairs and quality assurance service lines for healthcare product manufacturers.

TypeBroad incumbent
Description

ICON plc is a global CRO and healthcare intelligence company offering clinical, regulatory, and laboratory services. Comparable to Dor on regulatory submissions and clinical trial coordination, with much broader geographic and service coverage.

TypeBroad incumbent
Description

ProPharma Group provides regulatory affairs, compliance, clinical research, and pharmacovigilance consulting to pharma and medical device companies. Overlaps directly with Dor's RA, QA, and PV services, but with much broader international reach.

TypeBroad incumbent
Description

PharmaLex, now part of Cencora, is a global regulatory affairs, quality management, and pharmacovigilance services provider. Comparable to Dor across RA, QP, and PV service lines, but at much larger scale and broader geographic footprint, including Israel presence.

TypeEmerging player
Description

Biologics Consulting Group provides regulatory, quality, and compliance consulting to biologics, pharmaceutical, and medical device companies. Overlaps with Dor's RA and QA offerings but focuses more on FDA-facing regulatory work in the US market.

TypeBroad incumbent
Description

Parexel provides biopharmaceutical services including regulatory consulting, clinical research, and pharmacovigilance. Competes with Dor for RA and PV engagements from global pharma and medical device manufacturers, with deeper regulatory expertise across major markets.

TypeBroad incumbent
Description

IQVIA is the largest global provider of clinical, regulatory, and commercial services to life sciences companies. Competes with Dor for regulatory affairs and pharmacovigilance engagements, particularly on global master service agreements, though at vastly larger scale.

TypeOthers
Description

Tarius is a regulatory intelligence platform covering 100+ countries with a network of 300+ regulatory specialists, already a partner of Dor's. Functions as an enabling technology/intelligence vendor to Dor's regulatory affairs practice rather than a direct competitor.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 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 customers4 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 profile4 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

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles4 records

Each record includes

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

No data
Compliance6 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 →

Dor Pharmaceutical Services

Pharmaceutical Regulatory Servicesdor-ps.com

Dor Pharmaceutical Services firmographics

Firmographics
Name
Dor Pharmaceutical Services
Legal name
Novolog (Pharm Up 1966) Ltd.
Website
https://dor-ps.com
Company type
Private
Founded year
2011
Operating status
Operating
Headcount range
11–50 employees
Ownership category
akta.pro rank

Dor Pharmaceutical Services industry classification

Industry
Product category
Pharmaceutical Regulatory Services
NAICS
Professional, Scientific, and Technical Services (54), Scientific Research and Development Services (5417), Management Consulting Services (54161)
SIC
Services-Health Services (8000), Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC) (HLAGAHAM)
akta.pro secondary industry
Manufacturing, MSAT & Operations Staffing (API/Biologics/Cell & Gene) (HLAGAOAL)

Keywords

  • Pharmaceutical regulatory services
  • Quality assurance consulting
  • Medical device compliance
  • Pharmacovigilance services
  • Clinical trial coordination

Where Dor Pharmaceutical Services is headquartered

Location

Headquarters

HQ city
Modi'in
HQ country
Israel
HQ region
Middle East

Offices2 records

Markets served

Dor Pharmaceutical Services business model

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

Revenue model

  1. Regulatory Affairs and Registration Services: On-demand regulatory affairs outsourcing, including new drug registration, registration maintenance, appointed pharmacist services, and Marketing Authorization Holder (MAH) services for pharmaceutical, medical device, medical cannabis, cosmetics, and food supplement companies in Israel.
  2. QP and QA Services: Qualified Person (QP) certification, batch release services, and ongoing quality assurance management to help companies comply with GMP guidelines and Israeli Ministry of Health regulations.
  3. Labeling, Translation, and Printing Services: End-to-end product labeling and localization, including translation, graphic design, proofreading, and printing of packaging materials (leaflets, labels, folding cartons) for pharmaceutical, medical device, cosmetics, and food supplement products.
  4. Pharmacovigilance and Medical Information Services: Provided through sister company Medicalix, covering adverse event reporting, device vigilance, medical information, contact center services, and QPPV services for both marketed and clinical trial products.
  5. Clinical Trial Services: Full outsourcing of clinical trial coordination at leading Israeli medical centers, including protocol translation, informed consent form translation, regulatory submissions, and supply chain management.

Go-to-market motion2 records

Distribution channels1 record

Marketing channels5 records

Dor Pharmaceutical Services product offering

Product offering

Core offering

Dor Pharmaceutical Services is an Israeli B2B regulatory and quality services provider that supports pharmaceutical, medical device, medical cannabis, cosmetics, and food supplement companies with new drug registration, registration maintenance, Qualified Person (QP) and Quality Assurance (QA) services, GMP-certified labeling/translation/printing, pharmacovigilance, and clinical trial coordination. The company operates an outsourced regulatory affairs department model that extends or fully replaces client regulatory and QA teams on a flexible, on-demand basis, and serves as a one-stop-shop for navigating Israeli Ministry of Health requirements.

Product overview

Dor Pharmaceutical Services is a comprehensive regulatory and quality services company offering a unified platform of pharmaceutical services. The core offerings include Regulatory Affairs and Drug Registration, Qualified Person (QP) and Quality Assurance (QA) Services, Labeling/Translation/Localization with an in-house GMP printing plant, Clinical Trials Services, and Pharmacovigilance Services. The company operates across five industry verticals: Pharmaceuticals, Medical Devices (AMAR), Food Supplements, Cosmetics, and Medical Cannabis. Services range from new product registration and quality compliance to labeling production and clinical trial coordination. The company is part of Novolog Group's logistics division and serves over 300 customers since its founding in 2011.

Differentiator

Problem solved

Functional benefit

Brands

  • Medicalix: A sister company of Dor Pharmaceutical Services specializing in pharmacovigilance, device vigilance, and medical information services.

Products and services

  • Regulatory Affairs and Drug Registration Comprehensive regulatory services for obtaining marketing authorization for pharmaceutical products in Israel, including new drug registration, dossier examination, regulatory compliance, and registration maintenance for both innovative and generic drug manufacturers.
  • Qualified Person (QP) and Quality Assurance (QA) Services Certified QP batch release and QA services helping companies meet GMP guidelines and Israeli Ministry of Health regulations, including batch release, quality system establishment, GMP/GDP audit support, and ongoing quality management.
  • Labeling, Translation and Localization Services End-to-end product labeling and localization including translation into Hebrew, English, Arabic, and Russian, graphic design, proofreading via Global Vision technology, and printing of packaging materials (leaflets, labels, folding cartons) at the GMP-certified printing plant.
  • Clinical Trials Services Full outsourcing services for coordinating clinical trials at leading Israeli medical centers, including protocol translation, informed consent form preparation, regulatory submissions, and supply chain management.
  • Pharmacovigilance Services Adverse event reporting and monitoring services for pharmaceutical products and medical devices, including device vigilance, medical information, contact center services, and QPPV services for both marketed and clinical trial products, delivered through sister company Medicalix.
  • Medical Cannabis Regulatory Services Specialized regulatory services for Israeli medical cannabis companies covering facility establishment, validations, IMC-GMP certification, pharmacy services, product registrations, packaging materials, quality assurance, and clinical research for cultivation, production, distribution, and pharmacy operators.
  • Cosmetics Regulatory Services Regulatory affairs support for cosmetics in Israel, including product registration, labeling compliance, safety assessments, Product Information File (PIF) management, and support for adapting to the new Israeli Ministry of Health cosmetics directive and EC Regulation No 1223/2009.
  • Food Supplements Regulatory Services Comprehensive regulatory solutions for food supplement manufacturers, importers, and distributors to obtain product regulatory approval in Israel, covering dietary supplements, vitamins, nutritional supplements, herbal products, and homeopathic remedies.
  • Medical Devices Regulatory Services Focused regulatory solutions for medical device companies covering Israeli and international requirements, including AMAR (Medical Device Registration) with Israeli Ministry of Health, ISO 13485 compliance, device classification, import/export regulatory affairs, and quality management system support across all device classes.
  • GMP Printing and Relabeling Facility GMP-certified printing facility providing healthcare product labeling, including relabeling services and offset and digital printing on various substrates under cGMP, Israeli Ministry of Health, and multinational pharma company guidelines, managed by a qualified pharmacist and controlled by quality bodies.

Quantifiable outcome

  • Successfully accompanied IMC-GMP audits under new regulations for medical cannabis companies
  • +1 more outcomes

Companies that use Dor Pharmaceutical Services

Customer profile

Named customers4 records

Segments5 records

Ideal customer profiles4 records

Dor Pharmaceutical Services technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Dor Pharmaceutical Services partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered core.

  • Novolog Group (נובולוג)coreOthersDor is part of the Logistics Division of Novolog Group (TASE: NVLG), a senior strategic logistics partner of global pharma companies operating in Israel. Novolog Group employs more than 800 people and provides healthcare logistics, import, and distribution of medicines and medical devices, home healthcare and personalized healthcare, and medical information digital services.
  • MedicalixcoreTechnology or IntegrationMedicalix is Dor's sister company and the leading pharmacovigilance service provider in Israel. Dor outsources its pharmacovigilance (PV), device vigilance, and medical information (MI) services through Medicalix, enabling companies to comply with applicable local regulations for both marketed and clinical trial products.

Scale indicators3 records

Recent moves6 records

Expansion highlights6 records

Dor Pharmaceutical Services competitors and assessment

Company assessment

Emerging players

  • Regintel Consulting: Regintel is a smaller regulatory affairs consultancy serving pharma and consumer health companies. Comparable to Dor's regulatory service offering but with narrower geographic and therapeutic reach.
  • Biologics Consulting Group: Biologics Consulting Group provides regulatory, quality, and compliance consulting to biologics, pharmaceutical, and medical device companies. Overlaps with Dor's RA and QA offerings but focuses more on FDA-facing regulatory work in the US market.

Direct peers

  • Arriello: Arriello is a regulatory affairs, pharmacovigilance, and quality/compliance consultancy for pharma, biotech, and medical device companies across Europe and Israel. Closely comparable to Dor in service mix (RA, QP/QA, PV, labeling) and customer profile, with similar geographic focus.
  • The Weinberg Group: The Weinberg Group is a regulatory and quality compliance consulting firm serving pharma, biotech, and medical device clients. Directly comparable to Dor on regulatory affairs and quality assurance service lines for healthcare product manufacturers.

Broad incumbents

  • ICON plc: ICON plc is a global CRO and healthcare intelligence company offering clinical, regulatory, and laboratory services. Comparable to Dor on regulatory submissions and clinical trial coordination, with much broader geographic and service coverage.
  • ProPharma Group: ProPharma Group provides regulatory affairs, compliance, clinical research, and pharmacovigilance consulting to pharma and medical device companies. Overlaps directly with Dor's RA, QA, and PV services, but with much broader international reach.
  • PharmaLex (Cencora): PharmaLex, now part of Cencora, is a global regulatory affairs, quality management, and pharmacovigilance services provider. Comparable to Dor across RA, QP, and PV service lines, but at much larger scale and broader geographic footprint, including Israel presence.
  • Parexel International: Parexel provides biopharmaceutical services including regulatory consulting, clinical research, and pharmacovigilance. Competes with Dor for RA and PV engagements from global pharma and medical device manufacturers, with deeper regulatory expertise across major markets.
  • IQVIA: IQVIA is the largest global provider of clinical, regulatory, and commercial services to life sciences companies. Competes with Dor for regulatory affairs and pharmacovigilance engagements, particularly on global master service agreements, though at vastly larger scale.

Others

  • Tarius: Tarius is a regulatory intelligence platform covering 100+ countries with a network of 300+ regulatory specialists, already a partner of Dor's. Functions as an enabling technology/intelligence vendor to Dor's regulatory affairs practice rather than a direct competitor.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Dor Pharmaceutical Services social profiles

Digital presence

Dor Pharmaceutical Services compliance and trust

Trust signal

Compliance6 records

Dor Pharmaceutical Services financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Dor Pharmaceutical Services leadership team

Management profile

Number of profiles

Profiles4 records

Dor Pharmaceutical Services funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Dor Pharmaceutical Services 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 Dor Pharmaceutical Services

What does Dor Pharmaceutical Services do?

Dor Pharmaceutical Services is an Israeli B2B regulatory and quality services provider that supports pharmaceutical, medical device, medical cannabis, cosmetics, and food supplement companies with new drug registration, registration maintenance, Qualified Person (QP) and Quality Assurance (QA) services, GMP-certified labeling/translation/printing, pharmacovigilance, and clinical trial coordination. The company operates an outsourced regulatory affairs department model that extends or fully replaces client regulatory and QA teams on a flexible, on-demand basis, and serves as a one-stop-shop for navigating Israeli Ministry of Health requirements.

Is Dor Pharmaceutical Services a public or private company?

Dor Pharmaceutical Services is a private company. It is classified as corporate owned and is currently operating.

When was Dor Pharmaceutical Services founded?

Dor Pharmaceutical Services was founded in 2011. It employs 11 to 50 people.

Where is Dor Pharmaceutical Services based?

Dor Pharmaceutical Services is headquartered in Modi'in, Israel, in the Middle East region.

How does Dor Pharmaceutical Services make money?

Five revenue lines are on record. Regulatory Affairs and Registration Services are the primary driver. The others are QP and QA Services, labeling, Translation, and Printing Services, pharmacovigilance and Medical Information Services and clinical Trial Services.

Who are Dor Pharmaceutical Services's main competitors?

Emerging players on record are Regintel Consulting and Biologics Consulting Group. Direct peers are Arriello and The Weinberg Group. Broad incumbents are ICON plc, ProPharma Group, PharmaLex (Cencora), Parexel International and IQVIA. Tarius is listed as an others.

Does Dor Pharmaceutical Services have an API?

No public API is recorded for Dor Pharmaceutical Services.

What industry is Dor Pharmaceutical Services in?

Dor Pharmaceutical Services's product category is Pharmaceutical Regulatory Services. Its primary akta.pro industry code is HLAGAHAM, Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC), with a secondary code of HLAGAOAL, Manufacturing, MSAT & Operations Staffing (API/Biologics/Cell & Gene). Its NAICS code is 54 and its SIC code is 8000.

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