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The Pharmaceutical Testing component of CHEMISAR is located in the same premises with its dedicated facilities and capabilities for performing all tests, assays and analyses in compliance with:

• USP and BP specifications
• US FDA and HPB Canada Regulations
• Requirements for cGMP and cGLP
• USP and NF standards, reagents and references
• Method validation for all new methods/instruments
• Standard Operating Procedures
• Established Quality Control and Quality Assurance Procedures

Regular evaluations and audits are carried out by Government Agencies and Pharmaceutical Companies. In support of our rigorous QA/QC program, Chemisar Laboratories has established and maintains the highest level of performance in all of its projects. The program implements the policies to assure the validity and integrity of the analytical data. Major emphasis is placed upon qualifications of personnel and adequacy of facilities and equipment to achieve the highest degree of Precision and Accuracy of results.

Chemisar Laboratories meets all the requirements of a fully operational Quality Control / Quality Assurance Laboratory and provides a comprehensive range of analytical methods used in the Pharmaceutical industry for the measurement of drugs, impurities and excipients in Pharmaceutical preparations such as tablets, ointments and injectables. Amongst numerous assays and tests, we perform: