RemTech

What RemTech does

RemTech LLC is a privately held, Pennsylvania-based (Schwenksville) professional services firm founded in 2016, specializing in serialization, qualification and validation, construction management, and regulatory compliance consulting for the pharmaceutical, medical device, and biotechnology industries, with secondary exposure to the food industry. The firm delivers three core service lines: serialization and track-and-trace implementation (DSCSA compliance, serialization audits, EPCIS data management, and ongoing L4 system hosting and monthly support); qualification and validation services (IQ/OQ/PQ, cleaning validation, method validation, CMC product development support); and construction management plus staff augmentation, in which senior consultants are embedded in client teams. Technology inputs are conventional compliance tooling (alpha-numeric serialization, track-and-trace systems, GAMP documentation) and the firm also publishes educational content and participates in industry standards bodies (ISPE International Board, UGA Pharmaceutical Sciences Advisory Board).

RemTech generates revenue primarily through time-and-materials professional services engagements and project-based consulting fees, with a smaller recurring managed-services line (monthly L4 system hosting, master data management, and EPCIS file transmission support). Pricing is quote-based and not publicly disclosed. The go-to-market is sales-led and relationship-driven: principals Bob Matje and John Hartwig, supported by VP of Operations Austin McDonald, drive business development directly with enterprise pharma, med-device, and biotech clients across the United States, Europe, and Asia. Marketing channels are primarily the company blog, industry association participation, and client referrals, with named enterprise clients including Egalet, Trevena, Athenex, Fougera, Halocarbon, Iroko, Novum, Ultratap, SK Food Group, and Goodwin Biotechnology (GBI).

The firm has 11-50 employees, no disclosed outside funding, and is owned and controlled by its principals. Strategic positioning is reinforced by partnerships with Triad Unlimited (asset management and Relialtyics analytics) and Goodwin Biotechnology (biopharma CDMO Owner's Project Management), and by the principal-level involvement in ISPE and the UGA Pharmaceutical Sciences Advisory Board. The firm has not pursued acquisitions, IPOs, or external capital, and operates as a bootstrapped boutique consultancy.

Name

RemTech

Legal name

RemTech LLC

Website

https://remtechllc.com

Company type

Private

Founded year

2018

Operating status

Operating

Headcount range

11–50 employees

Short description

RemTech is a Pennsylvania-based, privately held professional services firm providing serialization, qualification and validation, construction management, staff augmentation, and regulatory compliance consulting to pharmaceutical, medical device, biotechnology, and food companies across the US, Europe, and Asia.

Ownership category

akta.pro rank

Product category

Pharmaceutical Consulting Services

NAICS

Research and Development in the Physical, Engineering, and Life Sciences (54171), Engineering Services (541330)

SIC

Services-Management Consulting Services (8742)

akta.pro primary industry

Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC) (HLAGAHAM)

Keywords

• Pharmaceutical consulting services
• Serialization implementation services
• GMP validation consulting
• Regulatory compliance consulting
• Construction management services

Headquarters

HQ city

Schwenksville

HQ country

United States

HQ region

North America

Offices1 record

Markets served

GTM type

B2B

Offering type

Services

Cost components

Personnel, Operations, Technology or R&D, Marketing or Sales, Others

Revenue model

1. Consulting Services: Professional consulting services including project management, construction management, engineering support, and strategic planning. Consultants work as part of client teams through staff augmentation or as project managers overseeing specific engagements.
2. Validation & Qualification Services: Qualification and validation services including Installation Qualification, Operational Qualification, Performance Qualification, cleaning validation, and method validation for pharmaceutical manufacturing equipment and processes.
3. Serialization Implementation: Serialization and track-and-trace system implementation including audits, data management, and ongoing support for Drug Supply Chain Security Act (DSCSA) compliance.
4. Client Onboarding and Monthly Support: Ongoing monthly hosting and support services including system hosting, engineering base level support, file management, master data management, and EPCIS data transmission management for serialization systems.

Pricing tiers

Go-to-market motion2 records

Distribution channels2 records

Marketing channels4 records

Core offering

RemTech is a professional services and consulting firm that delivers serialization implementation, qualification and validation, construction management, regulatory compliance, and staff augmentation services to pharmaceutical, medical device, and biotechnology manufacturers. The company combines cGMP compliance expertise with hands-on manufacturing technology and ongoing monthly support to help clients meet DSCSA and FDA requirements, achieve cost reductions of 20-30%, and execute capital and infrastructure projects.

Product overview

RemTech offers consulting services for the pharmaceutical, medical device, and biotechnology industries with a focus on serialization, compliance, and project management. Their core offerings include Serialization Services, Strategic Planning and Regulatory Support, and Specialized Services (validation and engineering). These are supplemented by modules for Construction Management, Staff Augmentation, CMC Product Development, and various audit services. The company also provides L4 Monthly Hosting for serialization systems and client onboarding support. RemTech positions itself as a turnkey solution provider combining cGMP compliance expertise with manufacturing technology and IP services.

Differentiator

Problem solved

Functional benefit

Products and services

• Serialization Services Implementation of serialization and automation solutions that assign unique alphanumeric codes to pharmaceutical units for product authentication, traceability, counterfeit reduction, and targeted recalls. Targeted at pharmaceutical manufacturers needing DSCSA compliance and supply chain visibility.
• Strategic Planning and Regulatory Support Consulting services to develop strategic plans aligned with regulatory requirements including FDA regulations, DSCSA compliance, and GMP standards for pharmaceutical, medical device, and biotechnology companies. Includes data management and supply chain optimization guidance.
• Qualification and Validation Services Qualification and validation services including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), cleaning validation, and method validation for pharmaceutical manufacturing equipment and processes. Includes GAMP documentation, SOPs, and URS authoring.
• Construction Management and Design Support Owner's Project Management and oversight of new construction projects from planning through execution, acting as client representative with engineering firms, contractors, and trade workers to ensure code compliance and on-time delivery.
• Staff Augmentation Placement of experienced consultants as full-time members of client teams to provide project management, engineering, validation, and technical expertise on an as-needed basis for extended engagements.
• CMC Product Development Assistance Comprehensive Chemistry, Manufacturing, and Controls (CMC) support for pharmaceutical product development, including technical operations and supply chain support for clients such as Trevena.
• Serialization and Track and Trace Audits Third-party and internal audits of serialization processes and supply chain tracking systems to ensure compliance with DSCSA requirements and industry standards, evaluating end-to-end traceability from source to consumer.
• Client Onboarding and Monthly Support Services Ongoing monthly managed services including L4 system hosting, engineering base-level support, file management, master data management, and EPCIS data transmission management for client serialization operations.

Quantifiable outcome

• Serialization solutions can reduce costs by 20-30%
• +2 more outcomes

Named customers10 records

Segments4 records

Ideal customer profiles3 records

Technology focussed No

API detail

Has API

No

API docs

API detail

Core technology

AI maturity

App detail

Feature4 records

Partnerships

Four partnerships are on record, tiered core and minor.

• Goodwin Biotechnology, Inc. (GBI)coreImplementation/ SI/ Consulting Partner · 10 February 2023RemTech partnered with Goodwin Biotechnology, a full-service biopharmaceutical Contract Development and Manufacturing Organization (CDMO), as it invests in infrastructure and expands capability. RemTech provides Owner's Project Management services and Quality and Compliance consultation services to assist GBI's continued success and growth in the biopharmaceutical market. This is an ongoing partnership supporting GBI's infrastructure investment and capability expansion.
• University of Georgia - Pharmaceutical Sciences Advisory BoardminorOthers · 15 September 2021Bob Matje, Principal at RemTech, serves as a member of the UGA Pharmaceutical Sciences Advisory Board at the University of Georgia, Atlanta campus. The board reviews college curriculum to ensure alignment with current technology and industry needs. This advisory role supports RemTech's commitment to education and the future of the pharmaceutical industry.
• Triad UnlimitedcoreStrategic or Co-development Partner · 1 September 2021RemTech partnered with Triad Unlimited to bring superior program packages to clients. Triad is an Asset Management Practitioner Consultancy Firm specializing in Life Cycle Asset Management, Maintenance, Reliability Engineering, and Long-Term Capital Planning Analysis. The partnership combines Triad's asset management framework and proprietary Relialtyics analytics technology with RemTech's project management, serialization, validation, and compliance expertise to offer comprehensive solutions that link asset issues to Critical Quality Attributes and Critical Process Parameters.
• International Society for Pharmaceutical Engineering (ISPE)minorOthers · 25 June 2020Bob Matje, Principal at RemTech, serves on ISPE's International Board of Directors. RemTech supports ISPE's educational mission and participates in industry initiatives. The partnership provides thought leadership opportunities and keeps RemTech connected to pharmaceutical industry developments and standards.

Scale indicators5 records

Recent moves5 records

Expansion highlights6 records

Direct peers

• Commissioning Agents Inc. (CAI): Engineering services firm specializing in commissioning, qualification, and validation for pharma, biotech, and medical device manufacturers. Direct overlap with RemTech's qualification/validation and construction management offerings.
• Tunnell Consulting: Life sciences-focused consulting firm serving pharma and biotech clients with operational, quality, and regulatory services. Highly comparable to RemTech in customer base (large pharma/biotech), service mix (validation, GMP, project management), and boutique scale.
• CRB Group: Engineering, architecture, and construction management firm dedicated to life sciences facilities. Comparable to RemTech on construction management, design support, and pharma facility build-outs, though at significantly larger scale.
• Körber Pharma: Supplier of pharma manufacturing equipment and serialization/track-and-trace solutions. Closely comparable to RemTech on serialization implementation and pharma supply chain compliance, though at much larger scale with hardware/software products.
• Clarkston Consulting: Management and technology consultancy serving life sciences, consumer products, and retail. Comparable to RemTech in serving regulated pharma/biotech buyers on operational, compliance, and supply chain projects.
• IPS-Integrated Project Services: Engineering and validation firm focused exclusively on life sciences, providing process engineering, facility design, and qualification services. Direct overlap with RemTech's construction management and validation services for pharma/biotech.

Broad incumbents

• TraceLink: Largest pharmaceutical track-and-trase network and serialization platform. Competes with RemTech's serialization implementation services by offering a software platform that customers (and partners like RemTech's L4 hosting) build on.
• Accenture Life Sciences: Global consulting and systems integration arm serving pharma, biotech, and medical device companies on regulatory, serialization, and digital operations. Competes with RemTech for enterprise pharma consulting engagements at vastly greater scale.
• Deloitte Life Sciences: Big Four advisory practice covering pharma serialization, regulatory compliance, and operations transformation. Adjacent competitor for large pharma programs where RemTech also competes.

Emerging players

• Triad Unlimited: Asset management consultancy specializing in life cycle asset management, reliability engineering, and capital planning for pharma facilities. Direct strategic partner of RemTech and partially overlapping on engineering support for pharmaceutical operations.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

Revenue estimate

Valuation estimate

Number of profiles

Profiles10 records

Funding overview

Funding rounds

Investors

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

M&A

Investments

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

Frequently asked questions about RemTech