We are committed to providing our clients with the highest quality in analytical (chemistry, chromatography, microbiology), consulting, stability, development and validation services. We strive to respect client timelines, as well as the accuracy and integrity of all data generated while performing tests or projects. We pride ourselves in ensuring our facilities, equipment, records and procedures are maintained in accordance with applicable regulatory and compendial requirements with respect to the Client’s specifications.
Neopharm Labs offers consulting services for quality assurance and regulatory requirements to the pharmaceutical industry. We assist our clients in various aspects of their quality assurance programs, including assisting them in meeting GMP requirements, developing Standard Operation Procedures (SOP), preparing for regulatory inspections and managing product and license submissions.
Our team at Neopharm Labs includes industry veterans with significant regulatory experience and capable of assisting our clients with respect to assessing requirements and developing:
- Stability programs in accordance to ICH Q1A, WHO and other regulatory requirements
- Validation and method transfers
- Regulatory compliance for Canada, US, Central & South America, Europe and Asian markets