Pharmaceutical Analytical Research and Development
Pharmaceutical laboratory research and development (R&D) services.
Intertek pharmaceutical analysis and project support laboratories help develop and validate methods, and provide solutions for clients with even the most difficult problems to overcome. Intertek pharmaceutical scientists recognize the importance of each client's research and technology, and measures customer satisfaction as the 'total quality' of every aspect and deliverable for an analytical project. We typically develop and validate cGMP compliant methods for the stability indicating analysis of drug products, APIs, packaging, extractables and leachables, cGMP quality control testing and process validations. Services and applications include:
- Method development and validation
- Method remediation (optimization and re-validation)
- Pre-formulation support
- Evaluation of API, excipients and API-excipient compatability
- Impurities and degradants
- API-packaging interactions
- Prototype evaluations
- Cleaning validations (specific and non-specific analyte determination)
- Extractables and leachables (organic and inorganic)
- Dissolution
- Apparatus' I, II and IV
- Apparatus IV expertise for slow-release and low solubility analytes
- Comparator studies, stability studies, release testing
- cGMP QC testing
- Impurity isolation, characterization and qualification
Pharmaceutical Research Services:
Request more information to see how Intertek can help your organization with Pharmaceutical Analytical Research and Development.