With a put together tenure across our corporations of approximately two hundred a long time and our market-regarded scientific and technological knowledge, we enable to make sure the safety of over 190 million sufferers and healthcare practitioners around the globe each year.
We recognize the varied difficulties and problems you deal with on your own strategy to obtaining GMP compliance during the pharmaceutical, biotechnology, ATMP and health-related unit producing industries - and we create realistic, achievable and cost-efficient options for you personally.
We support A huge number of companies, which include 17 of the very best 25 world wide pharmaceutical, biotech, and healthcare machine organizations, connect with the experts they require from the ideal workforce product.
Zero Defect: Producing an item which has no defects but guaranteeing the quality specifications and cutting down the defects into a degree of zero inside the initiatives.
Empowering sufferers to personalize their Health care and connecting them to caregivers has the possible to change the care shipping paradigm. IQVIA and Apple are collaborating to bring this thrilling future of personalized treatment on to devices clients have already got and use.
How can we do it? By Doing the job carefully with all your staff and by next our repeatable and reputable process.
Our GMP authorities have experience auditing devices against applicable regulatory and field expectations. Our industry experts get the job done along with you to apply the proper criteria based upon your requirements, the things to do or providers presented, and the phase of one's project.
Regulatory affairs is Regulatory Compliance Associates backbone. We exceed other pharma consulting corporations with market experts experienced in complexities in the pharmaceutical and biopharmaceutical industries.
To be a click here special assistance read more Each individual interim manager has staff back up at Valicare GmbH Business office, that is well-knowledgeable about The existing scenario at The shopper-web-site, making sure that she or he can switch the interim supervisor and not using a prolonged changeover period, if this will likely be important.
Our comprehensive-time GMP consultants respond promptly to all customer issues, which demonstrates one among our Main values.
Most FDA GMP consultants may have GMP consulting practical experience which is a vital qualification because they've got had possibilities to operate with several businesses and in different options. The importance of operational encounter, even so, really should not be forgotten.
All of our full-time GMP consultants are well-versed in Kellerman Consulting’s repeatable and reliable procedure. Our group’s collaborative society gives you the advantage of our collective knowledge with many profitable outcomes.
Acquiring IQVIA’s positions on crucial traits within the pharma and daily life sciences industries, which has a focus on EMEA.
We produce personalized projects in compliance with FDA / USDA regulatory needs and GMP certification requirements for every enterprise we serve.