TPM Laboratories
Independent contract testing laboratory offering analytical R&D, quality control testing, and stability storage/testing for pharmaceutical and chemical products. Operates a 6,000 sq ft facility in Cherry Hill, NJ with specialized containment for anticancer testing and regulatory registrations (FDA & DEA). Services emphasize method development/validation, compendial testing, stability programs, impurity profiling, and regulatory/audit support.
Industries
Nr. of Employees
small (1-50)
TPM Laboratories
1165 Marlkress Road, Unit D, Cherry Hill, New Jersey 08003
Products
Analytical Research and Development Testing Services
Provides analytical testing to support pharmaceutical and chemical product development and research.
Quality Control Testing
Performs testing to ensure pharmaceutical and chemical products meet quality standards and specifications.
Stability Storage and Testing Services
Offers storage and testing of pharmaceutical products to assess their stability over time under controlled conditions.
Analytical Research and Development Testing Services
Provides analytical testing to support pharmaceutical and chemical product development and research.
Quality Control Testing
Performs testing to ensure pharmaceutical and chemical products meet quality standards and specifications.
Stability Storage and Testing Services
Offers storage and testing of pharmaceutical products to assess their stability over time under controlled conditions.
Services
Method development, forced-degradation studies, method validation and validation reporting in accordance with FDA and ICH guidelines; method transfer services.
Testing of raw materials and finished products to compendial standards (USP/NF/BP/EP/JP) and client specifications.
ICH-aligned stability storage, client-specified storage conditions, stability testing, protocol/report preparation and data analysis.
Impurity and degradation profiling, preformulation studies and drug substance evaluation to support formulation and analytical strategies.
FDA deficiency response preparation, pre-approval inspection support, SOP generation, laboratory and vendor auditing, personnel/environmental monitoring.
Development and validation of process and cleaning methods and associated testing to support manufacturing validation.
Method development, forced-degradation studies, method validation and validation reporting in accordance with FDA and ICH guidelines; method transfer services.
Testing of raw materials and finished products to compendial standards (USP/NF/BP/EP/JP) and client specifications.
ICH-aligned stability storage, client-specified storage conditions, stability testing, protocol/report preparation and data analysis.
Impurity and degradation profiling, preformulation studies and drug substance evaluation to support formulation and analytical strategies.
FDA deficiency response preparation, pre-approval inspection support, SOP generation, laboratory and vendor auditing, personnel/environmental monitoring.
Development and validation of process and cleaning methods and associated testing to support manufacturing validation.
Expertise Areas
- Analytical method development and validation
- Compendial quality control testing
- Stability studies and ICH-compliant storage
- Impurity profiling and preformulation
Key Technologies
- High-performance liquid chromatography (HPLC/UHPLC)
- Gas chromatography (GC) and headspace analysis
- Diode-array and UV/visible spectroscopy
- Karl Fischer moisture titration