Intellex Acquires Expert by Big Village

We're thrilled to announce that Intellex has acquired Expert by Big Village, effective March 22, 2024. This strategic move enhances our capabilities and strengthens our commitment to delivering exceptional solutions to our customers.

Stay tuned for more updates on how this acquisition will benefit our clients and experts.

For inquiries or more information, please contact us at info@intellex.com.

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ID: 730278 Alabama, USA

Medical Device Sterilization, Medical Device QA, GMP Audit, Supplier Audit, SOP\’s

Expert, Consulting Principal, is highly regarded in the medical device and sterilization industries. Areas of expertise include: medical device sterilization (Radiation and EO), quality systems development and assessment, sterilization management, medical device regulations, supplier auditing, internal auditing, nonconformity investigation and…

ID: 730258 California, USA

Medical Device Regulatory Affairs, Quality Assurance, FDA 820 EU ISO 13485 510(k) & Medical Software

Lead and developed regulatory plan and strategy for Molecular Diagnostic System. Blood Analyzer, Gene Profiling Reagents, Blood Analyzer etc. Assembled with team regulatory submission and obtained 510(k) clearance, EU CE Mark, Health Canada, China SFDA, Mexico, Australia, South Korea, and…

ID: 730233 Pennsylvania, USA

Cardiac Electrophysiology, Cardiology Drugs, Pacemakers, Defibrillators, Cardiac Medical Devices

Expert. Expert is a board certified cardiac electrophysiologist (cardiologist with expertise in the diagnosis and treatment of all cardiac rhythm disorders) with over 20 years experience as a clinical investigator, IRB Chair, and high volume implanter of cardiac rhythm devices.…

ID: 729945 California, USA

Competitive Intelligence from Primary Sources in Pharmaceuticals, Diagnostics, and Medical Devices.

•Business research and development professional with a successful record targeting and developing Fortune 500 clients. •Founded pharmaceutical and information technology business intelligence firm and served as Business Development & Research Director for 15 years. •Expertise assessing the unique challenges facing…

ID: 729827 Pennsylvania, USA

Medical Device Accidents, Surgical Fires, Oxygen Safety, Medical Gas Piping, Failure Analysis

Eng. Expert has been conducting medical device accident investigations for 25 years and product failure analysis for more than 30 years. These failures sometimes involve the actual failure of a metal, plastic, or glass part or a failure of the…

ID: 729752 New Jersey, USA

Medical Device Design Control and Software Validation

Expert has extensive medical device engineering development and regulatory experience. He is a certified Lloyds of London ISO 9000 Lead Auditor and a member of the Westlaw Roundtable Expert Witness Network. His regulatory experience is primarily in product development, design…

ID: 729652 Indiana, USA

Patent Infringement, Implants, Medical Devices, Surgical Devices, Surgical Implants, FDA

Expert has expertise in certain medical devices and surgical devices. He also has expertise in certain medical implants and surgical implants.

ID: 729566 Illinois, USA

Food & Drug Administration Rules, Policies, Procedures for Medical Devices and Pharmaceuticals

Expert is an FDA compliance expert with 28 years experience in the field. He served the U.S. Food and Drug Administration as an Investigator concentrating in compliance for pharmaceuticals and medical devices as well as pre-market development of drugs and…

ID: 729459 Australia

Medical Device, Fabrication, White Goods, Automotive

Expert is a motivated, experienced, professionally qualified, results driven Manager with proven track record and strong, man management and team building skills. MSc in Manufacturing Management- Open University (UK). Professional Experience in: 1. Productivity and manufacturing efficiency improvements, through implementing…

ID: 729312 India

Regulatory Affairs/Registration Consultancy for Medical Devices/Drugs/IVDs/Food in Indian Market

Expert with a post graduate degree in Chemistry has been part of the team in the CDSCO, Government of India for framing of the Import Registration requirements for Drugs, Medical Devices and IVDs. Expert was the Medical Devices Reviewer for…

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