1. Definition of OOS and OOT Out of specification (OOS) is defined as a result that falls outside the predetermined specifications or established acceptance criteria set by the manufacturer and/or the laboratory. In simple terms, the result of a stability test conducted by a Quality Analyst (QA) should ...

FIFO (First-In-First-Out) & LIFO (Last-In-Last-Out) are methods used in managing inventory and financial matters involving the amount of money or raw materials of a company which has to have tied up within inventory of produced goods, raw materials, parts, components, or feed stocks. Used to manage ...

1. Responsibility: =>> The Company and its members are committed to provide a safe and healthy working environment and comply with all regulations for the preservation of the environment of the territory it operates in during the course of its operations. The Company and its members shall be committed ...

A pharmaceutical technology transfer can be defined as the transfer of scientific information, a capability or technological base associated with a drug or from a donor side (knowledge center) to a receptor side (pharmaceutical manufacturing plant) that implies a positive experience learned and perceived ...

“EPD is Committed to Our Patients, Doctors and Pharmacists. We are committed to delivering high-quality products to help people live healthier, fuller lives. This is achieved through dedication to quality and continuing effectiveness of the quality management system to meet customer and Regulatory ...

BEACON Pharmaceuticals Limited will be the leader to bring in innovative and high-tech pharmaceutical products at affordable price for its customer. Beacon will achieve this by embracing the following principles in all of its operations: => We shall consistently deliver high quality, safe, effective ...

Beximco Pharmaceuticals Limited Bangladesh seeks to become a leading producer of high quality generics in the domestic as well as overseas markets by adopting the following principles in its various operations. i) We shall be committed to continuous improvement of the Quality Management System by measuring ...

Good Manufacturing Practices (GMP) are a set of standards that pharmaceutical companies must adhere to in order to make safe and effective medicines. GMP requirements are based on the principles of quality, safety and efficacy. The most important aspect of GMP is quality. Pharmaceutical products must ...

Avant Sante Research Center Fermic Grupo Neolpharma Interquim S.A. de C.V. Sinbiotik Internacional S.A. de C.V.

– Vistin Pharma aims at being a responsive quality supplier of pharmaceutical products in compliance with the current guidelines for Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) in EU, USA and Japan. The quality will be secured through the entire chain from raw material ...