Full Analytical Services for Pharmaceuticals/Packaging Systems
Increasing regulatory compliance, in conjunction with decreasing time lines for drug development, is challenging pharmaceutical companies’ analytical resources. To avoid costly delays and to manage resources effectively, drug manufacturers can turn to West Analytical Services for extractable/leachable testing, pharmaceutical packaging testing, drug stability studies and medical device analysis.
With its in-depth knowledge of the interaction and compatibility of drug products with rubber, glass and plastic packaging components and its state-of-the-art analytical techniques, West has the resources to conduct tests cost effectively and efficiently. By relying on West's expertise, pharmaceutical companies can focus their resources on what they do best – discovering and developing new drugs – and don’t have to expend valuable resources to establish their own methods for testing extractables/leachables.
West Analytical Services has an extensive program for extractables/leachables testing. In addition, our experience in analytical testing and packaging technology makes West the perfect choice for your analytical needs including stability studies and routine analysis. With the need to get to market quickly, why tie up your critical resources? Let West use its experience and expertise for your analytical requirements so that you can focus on developing new drug products.
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The Benefits of West Analytical Services
- Customers can minimize cost and development time because West has established many base methods for rubber, glass and plastic extractables
- West Analytical Services team has vast experience with multi-materials testing
- West Analytical Services has completed numerous extractables/leachables tests for pharmaceutical industry clients
- West Analytical Services provide unique test methods for packaging
- A technical specialist and project coordinator are assigned to every client study
- West Analytical Services can develop study-specific protocols
- Technical consultation for protocols, testing and study results
Laboratory Highlights and Capabilities
- FDA registered (#2531777), GMP facility
- A technical specialist and project coordinator are assigned to every project
- Packaging extractables and leachables expertise
- Unique test methods for packaging
- Stability testing and stability storage
- Method development and validation
- Compendial testing
- Rush service available
- DEA Class I – V
- Potent/Cytotoxic drug testing capabilities
- Full technical support staff
- Protocol design capabilities