At Regulatory Compliance Associates, we provide the pharma consulting knowledge and pharma consultants needed to guidebook you from the good quality compliance approach.

Their first-hand experience and insights from the sphere established us aside, making it possible for us to provide Extraordinary company grounded in sensible understanding.

As your companion, we can negotiate the possible assessment minefield of regulatory compliance solutions with insight, hindsight, along with the distinct advantage of our breadth and depth of information and regulatory compliance consulting. We offer the subsequent pharma consulting regulatory affairs providers for pharmaceutical providers.

We realize the complexities of functioning a lifestyle science business enterprise and have areas of experience that come with each individual side of R&D, operations, regulatory affairs, top quality, and production.

“We knew if we planned to get wherever we wished to go with our enterprise and securing several of All those huge clients, that we required to have SQF certification. After i first began conversing with Kellerman Consulting, I knew they had been professionals.

We have an understanding of the complexities of jogging a everyday living science business and possess parts of expertise that include each and every aspect of R&D, functions, regulatory affairs, high-quality, and production.

We have been able to not merely knowledge these world-wide polices, but will also of delivering strategic alternatives that keep in mind the two global and native compliance needs.

World wide supply chain disruption and API scarcity will pressure the market to diversify sourcing destinations and establish new supplier networks – all though delivering true-time, total-solution visibility and traceability.

To be a Specific provider Just about every interim supervisor has personnel back again up at Valicare GmbH Business, who's very well-knowledgeable about The present condition at The client-site, in order that they can replace the interim supervisor without a very long changeover period, if this will be needed.

Upon ask for, the respective regulatory authority will conduct an on-web site inspection to confirm compliance with nationwide law and EU GMP prerequisites.

Most FDA GMP consultants will likely have GMP consulting working experience which is a crucial qualification considering the fact that they have got experienced possibilities to operate with many businesses and in several settings. The importance of operational experience, nonetheless, should not be neglected.

We leverage Innovative technology and a powerful here Call community to rent talent that will incorporate new dimensions to your company.

Developing IQVIA’s positions on vital developments from the pharma and lifetime sciences industries, which has a concentrate on EMEA.

The laws process bordering pharmaceutical check here businesses could be tough for even one of the most seasoned industry veteran to be familiar with. Just one misstep could signify significant and Long lasting consequences for your small business.