PBE is a Canadian leading consulting company specializing in cGMP compliance to federal and provincial regulations, in Biotech, Pharma, Vaccine, & Life Science industries.

Since 2007, PBE has empowered scientists, engineers, revolutionaries and facility owners to make their goals come true in an ever-changing world. Founded in 2013, PBE Expert (Pharma Bio Expert) has quickly emerged as a leader in delivering comprehensive EPCMV Turnkey projects, encompassing services such as Engineering, Quality Assurance, Validation, and PAI. Our focus is primarily on life science, biotech, vaccine, and pharmaceutical sectors. With more than 30 years of collective experience, we have successfully executed over 300 GMPCMV pharmaceutical projects across a broad spectrum of areas including Fill & Finish (F&F), Biotechnology, Vaccines, Intravenous solutions (IV), Solid Dosage Forms (SV), High Volume Parenteral (HV), Single-Use Systems (SU), Pre-filled Syringes (PFS), Blow-Fill-Seal (BFS), Sterile, Oncological, and Oral Solid Dosage (OSD).

We understand that ensuring compliance can be a really challenging and complex process, especially in the pharma and biotech industries, however it is critical to ensure the safety and effectiveness of products.

PBE has Health Canada, US-FDA, EMA and MAPAQ (Ministère de l'Agriculture, des Pêcheries et de l'Alimentation du Québec) SME Experts within their team.

OUR APPROACH We work with our clients for the long-term, taking the time upfront to understand their business and workforce requirements to ensure commercial outcomes are achieved. CPMT certified, we hire and train the top talent in the pharmaceutical industry, to build a strong team of SME (Subject Matter Experts) with the skills you need to achieve your goals with peace of mind.

Key Services: Facility Engineering, Validation (pharmaceutical), CQV, QA, GMP Design, RCA & Investigations, CAPA, PM, Procurement, pre-approval inspections & more.

Visit www.pbe-expert.com