- Becoming a member of our IGAP program/ Audit report library is free for suppliers/manufacture. Our skilled and capable auditor will conduct complete site audit of supplier masking significant number of molecules/goods (if not presently done) without any cost to supplier and detailed audit report shall be well prepared.

We have an understanding of the varied difficulties and issues you encounter on your own strategy to acquiring GMP compliance during the pharmaceutical, biotechnology, ATMP and health-related system manufacturing industries - and we develop functional, achievable and price-powerful methods for you.

IQVIA Decentralized Trials supply intent-designed clinical services and systems that interact the appropriate clients wherever They are really. Our hybrid and fully Digital methods are actually used a lot more than any Some others.

It’s a pharma consultancy Launched by regulatory compliance executives from the pharmaceutical marketplace. Each pharmaceutical sector consultant within the Regulatory Compliance Associates group knows the unique internal workings on the regulatory approach.  

“We understood if we desired to get wherever we planned to select our business enterprise and securing a number of Those people big clients, that we necessary to have SQF certification. After i to start with started out conversing with Kellerman Consulting, I knew they ended up specialists.

On top of that, Every single Regulatory Compliance Associates pharma consulting Professional understands compliance enforcement. We’ll put together an extensive pharma consulting technique to guide with your remediation attempts, drive continual enhancement, and manage regulatory compliance with the laws.

We have been effective at not merely understanding these world-wide rules, but will also of giving strategic methods that take into account each world and local compliance check here necessities.

Corporate Location procedures for advancement as a result of restructuring, effectiveness enhancements and scaling up of functions.

We could consequently offer you this consulting support in Every mode usual available in the market. The design assessment can often be completed without having a corresponding on-web page presence, exclusively dependant on the pharma consultants in India specialized documentation about the overall and detailed arranging of the installation.

Our industry experts performs 3rd party evaluation and gap Investigation that has a quantified Resource to evaluate the organization’s condition of regulatory compliance. We assistance the companies in developing CAPA for deficiencies lifted by regulatory inspections.

Using a combined tenure throughout our companies of nearly 200 a long time and our marketplace-recognized scientific and technological expertise, we assistance to ensure the security of around one hundred ninety million individuals and healthcare practitioners world wide each and every year.

It leads to enhanced current market pace and enhanced transparency and accountability in the course of various organizations linked to formulation (throughout multiple dosage kinds), API and biosimilar.

- The audit report shall be then available inside our Audit report database that may be accessible to any of the consumers. We'll get authorization with the supplier just before sharing reviews for the customers.

Acquiring IQVIA’s positions on important developments inside the pharma and existence sciences industries, using a give attention to EMEA.