Good Laboratories Practice (GLP) Services for Pharmaceuticals CompaniesGood Laboratory Practice Good Laboratory Practice (GLP) is a quality system applied to non-clinical health and environmental safety studies during the development of new products such as medicines, cosmetics, food products, industrial chemicals and pesticides. GLP provides assurance that study data submitted to regulatory authorities is accurate, valid, [...]
Computer System Validation for Pharmaceutical Industry Computer System Validation/ Compliance (CSC) Computer systems validation (CSV) is an essential requirement within the pharmaceutical, biotech and medical device industries. Over the past decades, the life science industry has progressively introduced computer systems to support clinical trials, manufacturing, control, and logistics processes. As a consequence, these computer systems [...]
Good Clinical Practice(GCP) Support Services for Pharma and Biotech Industries Good Clinical Practice Pharmatek team encompasses of qualified and trained subject matter experts (SME) to deliver quality services meeting the regulatory compliance. Our highly experienced, trained, and competent team of specialist GCP auditors has conducted audits in a broad range of therapeutic areas including oncology, [...]
Good Pharmacovigilance Practice (GVP) Services for Pharmaceutical Industry Good Pharmacovigilance Practice (GVP) Good Pharmacovigilance Practice (GVP) is the minimum standard for continuously monitoring, collecting and providing patients, healthcare professionals, and the general public with timely information about the safety of medical products. Pharmatek feel pride to provide patient centric responsive and agile services to our [...]
Senectus accumsan malesuada cursus dapibus sem primis cubilia, per potenti fermentu massa pulvinar turpis taciti, pellentesque.