We are an independent consultancy firm of professionals from various scientific, technical, IT, business and regulatory backgrounds with experience in GMP-regulated industries such as innovative pharmaceuticals, biologics development and manufacture, generics and medical device industries.
We are specialized in providing QA, compliance, regulatory, IT, project management and productivity improvement services to the pharmaceutical, biotechnology and medical device industries.
We focus on providing customized services to our clients in an effective and cost efficient way as well as support Pharmaceutical and Biotechnology companies in solving specific problems relevant to biologic raw materials.
Our consultants have successfully executed mandates in various parts of the world (North America, East Europe, MENA and more), working with both large and smaller life sciences organizations.
Our consultants apply decades of experience in the pharmaceutical, biologicals & medical device development, manufacturing, business development, market access and supply to develop solutions that work for you.
Our approach is specifically designed around each of your precise goals and unique situations to provide solutions that exceeds your expectations.
MBBioservices enjoy strategic collaborations with quality auditors, consultants, experts in Validation, IT management/structure and bioprocess professionals in key regions of the world allowing seamless project transition, and team integration.
MBBioservices assist organizations across several aspects of their operations. From innovative and strategic analysis to cross-functional operational assistance and quality compliance.
Because of our flat organizational structure, our consultants enjoy incomparable freedom of operations, resulting in a deeper commitment with our clients, from both technical and human aspects.