Passionate – Dedicated – Professional
Acculab group is a leading manufacturer of laboratory and medical instruments
Established in 2004 through the merger and acquisition of several companies, Acculab Group has become a global leader in providing advanced scientific solutions. With a strong presence in the America, Canada, Europe, Middle East and Africa region.
strong presence across the Americas, Canada, Europe, the Middle East, and Africa
Acculab Group is dedicated to empowering laboratories, healthcare facilities, and industries with state-of-the-art equipment and technologies. Our commitment to quality, precision, and innovation has positioned us as a preferred partner for professionals in diverse fields, from healthcare and pharmaceuticals to environmental science and industrial applications.
Acculab Group is committed to
pioneering innovation in the field of laboratory and medical equipment. The following companies are member companies of Acculab Group
We are committed to delivering the highest standards of quality and excellence. We are proud to hold ISO/IEC 17065:2012 accreditation, granted by British Columbia Inspection & Certification (BCI), confirming that our organization meets the international requirements for bodies certifying products, processes and services. This accreditation covers our Supply of Laboratory Equipment & Scientific Instruments, including Molecular Biology Equipment, Histopathology Equipment and Medical Laboratory Equipment, and supports our presence in international markets.
Key Highlights:
Standard: ISO/IEC 17065:2012 – Conformity Assessment (Requirements for Bodies Certifying Products, Processes and Services)
Issue Date: September 14, 2026
Expiry Date: September 13, 2029
Certification Body: British Columbia Inspection & Certification (BCI)
Furthermore, we are proud to hold ISO 13485:2016 certification for our Medical Devices Quality Management System, awarded by Royal Impact Certification Ltd. (RICL) and recognized under the International Accreditation Forum (IAF) through the United Accreditation Foundation (UAF). This certification underscores our dedication to quality and safety across our Supply of Laboratory Equipment & Scientific Instruments, including Molecular Biology Equipment, Histopathology Equipment and Medical Laboratory Equipment.
Key Highlights:
Standard: ISO 13485:2016 – Medical Devices Quality Management Systems
Initial Certification: September 9, 2026
Valid Until: September 8, 2029
Certification Body: Royal Impact Certification Ltd. (RICL)
In addition, we hold ISO 9001:2015 certification for our Quality Management System, awarded by Royal Impact Certification Ltd. (RICL) and recognized under the International Accreditation Forum (IAF) through the United Accreditation Foundation (UAF). This certification reflects our ongoing commitment to consistent quality, customer satisfaction, and continual improvement across our Supply of Laboratory Equipment & Scientific Instruments, including Molecular Biology Equipment, Histopathology Equipment and Medical Laboratory Equipment.
Key Highlights:
Standard: ISO 9001:2015 – Quality Management Systems
Initial Certification: September 11, 2026
Valid Until: September 10, 2029
Certification Body: Royal Impact Certification Ltd. (RICL)
We are also proud to hold CE certification (Certificate of Compliance), granted by British Columbia Inspection & Certification Management (BCI), confirming that our products are in full conformity with the requirements of the CE Marking Directives and Regulations applicable within the European Union. The certification body reviewed the technical documentation, test assessments, design evaluation, manufacturing process and test reports of our products, confirming they meet the essential health, safety and environmental protection requirements of the EU. It covers 50 registered product groups across our Supply of Laboratory Equipment & Scientific Instruments, including hematology, chemistry, immunoassay, coagulation and blood gas analyzers, centrifuges, blood bank and medical refrigerators and freezers, microscopes, biosafety cabinets, incubators, autoclaves, thermal cyclers and real-time PCR, histopathology equipment (microtomes, cryostats, tissue processors, slide stainers and embedding systems) and dental equipment.
Key Highlights:
Standard: CE Marking – Conformity with applicable EU Directives and Regulations
Issue Date: September 23, 2026
Expiry Date: September 22, 2029
Surveillance Audits: Before September 23, 2027 and September 23, 2028
Scope: 50 registered product groups, Class 1a
Certification Body: British Columbia Inspection & Certification Management (BCI)
Verification: www.bcicert.org
