ProPharma Group – Regulatory Affairs, Life Science Consulting, Pharmacovigilance and Medical Information

Science and technology have grown increasingly integrated, necessitating expert knowledge to complete any project’s development lifecycle. Thanks to access to the newest technologies and trends, ProPharma Group’s consultants of technology use integrated strategies to discover the most up to standard technology solutions for its customers. It recognizes that there is no such thing as a one-size-fits-all approach for companies to take to science and technology, and so it doesn’t approach its initiatives as if there is.

It is the world’s top-rank provider of regulatory, clinical, and compliance services from a single source. As an independent provider, it supports the pharmaceutical, biotechnology, and medical device industries. ProPharma Group offers a team of professionals who cover a full portfolio of life science consulting, regulatory sciences, pharmacovigilance, medical information services, and clinical research solutions to assist customers in overcoming challenging issues in a changing regulatory environment.

ProPharma Group’s objective is to improve the health and safety of its patients, and it is committed to providing the greatest level of service throughout the lifespan of the client’s product.

ProPharma Group was established in the year 2001 as a major provider of validation and other associated life science consultancy services in the pharmaceutical, biotechnology, and medical device industries. Today, it is recognized as one of the most innovative providers of specialist consulting services, thanks to its global team of trusted life science consulting experts.

Its team of compliance and quality experts brings a wealth of knowledge to life science consulting, utilizing established and patented project management approaches to assist customers in bringing products to market. Whether a company needs short- or long-term hiring, GoodxPractice (GxP) consulting services, or quick remedial support to get a project back on track, ProPharma Group tailors a solution to match its customers’ specific requirements.

ProPharma Group’s presence can be seen across 6 different continents, providing crucial support services to each of its clients. It has a growing workforce of over two thousand specialists that, with the support of regional competence, deliver some of the best quality services on a worldwide scale.

It also supports its clients with proven resource management tools and services. With its clinical project management software, ProPharma Group is able to provide its clients with a powerful but simple application for Biopharma companies all around the world.

“Working in close partnership with our clients to improve the health and safety of patients, our global teams are committed to quality and excellence in everything we do to support clients throughout the full product lifecycle,” says Michael Stomberg, the CEO of ProPharma Group.

ProPharma Group’s objective is to streamline the pharma regulatory process in order to allow any business to prosper. It’s professional regulatory consulting and FDA compliance team has an unrivaled breadth and depth of knowledge about the FDA and EMA regulatory frameworks and can help a company achieve its regulatory and business targets.

It continues to build upon its strong foundation of regulatory science with its acquisitions that help deepen its service capabilities and further globalize. Its seasoned regulatory sciences team has over 30 years of expertise strategizing feasible and efficient medication and device development routes with regulatory bodies in the US and Europe to achieve successful outcomes.

ProPharma Group aims to improve the overall patient health and safety every step of the way. Right from the early concept development stage through each clinical phase, the product release, and the commercialization of the products and services, ProPharma Group partners with all of its clients to tackle any complex challenges that may come their way.