Obtaining and maintaining GMP Certification is a prerequisite if your goal is to operate within the pharmaceutical or biotechnology industries. It is one of the steps required to ensure that the company’s products are safe, compliance is obtained, and relevancy in the international market is a…
To ensure quality, safety and regulatory compliance, pharmaceutical and biotech companies need to adhere to GMP standards. Structured procedures are maintained with the help of a GMP compliance audit checklist. It guarantees that no important requirement is missed, maintaining operations’ …
The purpose of computer system validation (CSV) is to guarantee confidence in the data captured, processed, reported or stored on computerised systems. A validated system ensures accurate results and reduces any risks to data integrity.
The extent of validation activities should be defined bas…
Compliance in pharmaceuticals and biotech is non-negotiable. A GMP compliance audit checklist is a tool for regulatory approval and assures you that every process, product and protocol meets the highest safety and quality standards. Regulatory agencies like the FDA and EMA require strict complia…
For pharmaceutical and biotech companies, obtaining a Wholesale Dealer Authorisation (WDA) licence is essential for regulatory compliance. It ensures businesses meet UK standards for distributing medicines, medical devices and healthcare products.
A WDA licence ensures compliance with regulato…
In the pharmaceutical and biotech industries, maintaining the integrity of temperature-sensitive products is crucial. Temperature mapping services in London ensure storage conditions stay within required ranges, supporting quality assurance and regulatory compliance.
Temperature mapping ensure…
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