PMRS, Inc.
PMRS, Inc. is a full-service pharmaceutical contract manufacturer dedicated to ensuring client success through expertise, quality, and innovation. With over 30 years of experience, state-of-the-art facilities, and a comprehensive range of services including manufacturing, analytical testing, and quality assurance, PMRS strives to deliver high-quality pharmaceuticals efficiently and cost-effectively. The company emphasizes continuous improvement, environmental responsibility, and customer satisfaction, supporting projects from discovery through commercialization.
Industries
Nr. of Employees
small (1-50)
Patents
Products
Pharmaceutical Contract Manufacturing and Analytical Services
Comprehensive pharmaceutical production, clinical supply, commercial-scale manufacturing, and advanced analytical testing services provided out of a custom-built cGMP facility.
Release Testing Services
Extensive analytical support and release testing for in-process products as well as finished dosage forms.
Stability Testing and Storage Services
Onsite stability study storage and testing utilizing ICH compliant stability environmental chambers backed up with emergency power.
Phase I, II, and III Clinical Supply Manufacturing
Clinical supply manufacturing services supporting early to late-stage pharmaceutical development.
Method Development and Validation Services
Validation of analytical methods in various product formulations including tablets, capsules, creams, and extrusions in compliance with FDA and ICH guidelines.
Commercial Scale Manufacturing
Full-scale commercial production and manufacturing of pharmaceutical products.
Pharmaceutical Contract Manufacturing and Analytical Services
Comprehensive pharmaceutical production, clinical supply, commercial-scale manufacturing, and advanced analytical testing services provided out of a custom-built cGMP facility.
Release Testing Services
Extensive analytical support and release testing for in-process products as well as finished dosage forms.
Stability Testing and Storage Services
Onsite stability study storage and testing utilizing ICH compliant stability environmental chambers backed up with emergency power.
Phase I, II, and III Clinical Supply Manufacturing
Clinical supply manufacturing services supporting early to late-stage pharmaceutical development.
Method Development and Validation Services
Validation of analytical methods in various product formulations including tablets, capsules, creams, and extrusions in compliance with FDA and ICH guidelines.
Commercial Scale Manufacturing
Full-scale commercial production and manufacturing of pharmaceutical products.
Services
Facility-based contract manufacturing across clinical phases and commercial production for solid, semi-solid, and liquid dosage forms, including high-potency containment and process scale-up.
On-site analytical laboratory services including method development and validation, release and stability testing, elemental impurity analysis via ICP-MS, microbiological testing, and LIMS-managed reporting.
Quality systems and regulatory support including SOP/document system development, QA audits, CAPA and change control management, IQ/OQ/PQ validation support, and electronic quality/records systems.
Facility-based contract manufacturing across clinical phases and commercial production for solid, semi-solid, and liquid dosage forms, including high-potency containment and process scale-up.
On-site analytical laboratory services including method development and validation, release and stability testing, elemental impurity analysis via ICP-MS, microbiological testing, and LIMS-managed reporting.
Quality systems and regulatory support including SOP/document system development, QA audits, CAPA and change control management, IQ/OQ/PQ validation support, and electronic quality/records systems.
Expertise Areas
- Contract pharmaceutical manufacturing
- Analytical method development and validation
- cGMP quality assurance and regulatory compliance
- Process Analytical Technology and in-process control
Key Technologies
- High-performance liquid chromatography (HPLC)
- Rapid-resolution liquid chromatography (RRLC)
- Inductively coupled plasma mass spectrometry (ICP-MS)
- Near-infrared spectroscopy (NIR) for PAT and material ID
News & Updates
2025 Controlled & Modified Release Summit
May 7-8, 2025 – Hyatt Regency New Brunswick, New Brunswick, NJ.
CPHI Americas 2025
May 20-22, 2025 – Pennsylvania Convention Center, Philadelphia, PA.
30+ Years of Excellence
Providing world-class pharmaceutical services since 1994.
2025 Controlled & Modified Release Summit
May 7-8, 2025 – Hyatt Regency New Brunswick, New Brunswick, NJ.
CPHI Americas 2025
May 20-22, 2025 – Pennsylvania Convention Center, Philadelphia, PA.
30+ Years of Excellence
Providing world-class pharmaceutical services since 1994.