Laura with Kellerman Consulting is simply great. She is extremely practical, easy to work with and got us via our GMP audit that has a far better score than we anticipated. Also, the Firm of each of the documents Kellerman Consulting delivered us with is superb.

With long lasting placement through the FDA Team, it is possible to carry out a few Major objectives: lower the cost of talent identification and shipping and delivery, get the certain top quality of new hires, and mitigate the risks of recruiting new staff. 

Get speedy, versatile use of certified cGMP specialists who can strike the ground jogging and right away increase price to your organization through a whole-time deal or contract-to-retain the services of team augmentation product. FTE Recruitment

To start the Regulatory Compliance Associates scoping approach currently, please enter your data in the blue kind underneath and click the post button at The underside of your webpage.

"Strengthening human overall health calls for brave thinkers that are ready to investigate new ideas and Create on successes. Unleash your probable with us.

Whether or not you’re while in the product setting up, improvement or pharmaceutical lifecycle management stage or need a remediation approach for any compliance disaster, Regulatory Compliance Associates get more info will information you through each pharmaceutical consulting stage in the regulatory approach.

To start the Regulatory Compliance Associates scoping system now, you should enter your information and facts from the blue kind down below and click the submit button at The underside in the webpage.

Together with the FDA Team as your resourcing husband or wife, you can certainly improve or minimize your workforce as requirements fluctuate—all although obtaining Price efficiencies in recruiting, screening, and onboarding team.

No matter if you need a devoted GMP consultant, sparring spouse or enable finding the right Resolution on your approach, we possess the know-how and encounter to optimize your functions.

IQVIA Decentralized Trials deliver function-built clinical companies and systems that have interaction the best individuals anywhere They can be. Our hybrid and completely Digital methods are already utilised more than any Some others.

We more info perform with our clients to audit and develop management programs that enable greater transparency over the organization, notify the development of new approaches to your broad range of regulatory and tax compliance, and assistance strengthen efficiency.

We realize the complexities of operating a life science business and have places of expertise that come with each individual side of R&D, functions, regulatory affairs, high-quality, and producing.

Anxious your good quality procedure would not mirror FDA expectations? Link with former FDA and sector specialists who definitely have extensive familiarity with FDA's current inspection methods and expectations that transcend the phrases of regulation.

Our high quality, producing, CAPA, and supplier good quality authorities perform in depth procedure assessments and analyses to guarantee all compliance gaps are closed regardless of wherever They might be.