Good Manufacturing Practices (GMP) are a set of regulations and guidelines ensuring the consistent quality, safety, and efficacy of products in industries such as pharmaceuticals, food, cosmetics, and medical devices.
Good Laboratory Practices (GLP) are a set of principles intended to ensure the quality, integrity, and reliability of non-clinical laboratory studies, especially in research and safety testing for pharmaceuticals, chemicals, and environmental studies.
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Equipment Qualification (EQ) is the process of ensuring that instruments and equipment used in manufacturing, laboratories, and regulated industries perform consistently and as intended.
Cleaning Validation is a documented process that ensures manufacturing equipment and facilities are cleaned to prevent contamination, cross-contamination, and residues that may impact product quality and safety.
Process Validation is a systematic approach used in manufacturing to ensure that a process consistently produces products meeting predetermined quality standards.
Drug Regulatory Affairs (DRA) is a specialized field within the pharmaceutical and biotechnology industries that ensures compliance with regulations and guidelines for drug development, approval, manufacturing, and marketing.
Good Pharmacovigilance Practices (GVP) are a set of guidelines established to ensure the safety monitoring of medicines throughout their lifecycle.
Temperature Mapping is a critical process in regulated industries (such as pharmaceuticals, biotechnology, and food storage) to ensure that controlled environments maintain the required temperature conditions.
Calibration is the process of verifying and adjusting the accuracy of measuring instruments to ensure they provide reliable and consistent results.
A Pharmaceutical Quality System (PQS) is a structured framework ensuring the consistent production of high-quality pharmaceutical products that meet regulatory standards, patient safety, and efficacy requirements.
Vendor Management is a critical process in the pharmaceutical industry to ensure that suppliers, contractors, and third-party partners meet regulatory and quality standards
Annual Product Quality Review (APQR) is a regulatory requirement for pharmaceutical companies to assess the quality, consistency, and compliance of a drug product over the past year.
Pharmaceutical gases, such as oxygen, nitrogen, carbon dioxide, compressed air, and argon, play a critical role in pharmaceutical manufacturing.
