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: 725163 Florida, USA

Medical Device Regulatory Support, Medical Device Registration, etc.

Expert is a Regulatory and Quality Consultant with strong team building skills for high technology corporations. A hands-on career of increasing leadership positions with a broad range of responsibilities in manufacturing, regulatory affairs and new product introductions. A committed professional…

ID: 724290 California, USA

Electronic and Mechanical Device Reliability, Failure Analysis, Risk and Safety Assessment

Expert is an expert in the fields of reliability, risk, and safety assessment. He performs electronic and mechanical device reliability analysis, failure analysis, failure modes and effects analysis, and fault tree analysis. Expert is an expert in the fields of…

ID: 724264 Minnesota, USA

Medical Device Design and Manufacture

Expert has over 25 years experience in the conception, design, and manufacture of medical devices. Experience ranges from high volume disposables to low volume implantables. Beginning as a manufacturing engineer responsible for all facets of device development and manufacture Expert…

ID: 723350 California, USA

Adhesives for Medical Device, Biotech, Pharmaceuticals, Aerospace, Materials Science, QA, QC

With a PhD in organic chemistry expert has spent over 25 years developing adhesives, resins and advanced composites for a variety of applications. He started at the bench chemist level and worked his way up into R&D management. Some of…

ID: 723272 New Jersey, USA

Parasitology, Immunology, Microbiology, Bioterror Agents, Grant Writing, Med Writing, Expert Witness

Expert has extensive experience in the preparation and submission of 510(k) documents to the FDA for approval of Class II medical devices. His first work in 510(k) preparation and submission was in 1987 for acceptance of a rapid immunoassay for…

ID: 723204 Illinois, USA

Biomedical Engineering; Medical Devices

IP Projects Catheter stabilizing device Dental Instrument Implant Seeds Intrauterine pressure catheter Vascular Catheters (3) Over 30 years experience in medical product design and development experiences in Anesthesiology, Assistive Technology, Cardiovascular, Catheters, Critical Care, Endoscopy, Implants, Instruments, IV Systems, Home…

ID: 722720 Wisconsin, USA

Business Plans

Array Expert has developed and implemented chemical safety procedures for several clients, including a chemical recycling facility, and metal finishers using strong acid and alkaline chemistries, etchants, and electropolishing chemicals in their manufacturing and/or wastewater treatment processes. Activities include safety…

ID: 722626 North Carolina, USA

PK/PD Modeling and Simulation; Nonclinical and Preclinical Statistics; Experimental Design

He managed group of 5 biostatisticians working on Phase I and PK/PD trials. His responsibilities included protocol design, statistical analysis plan writing, specification writing, and delivery of product to customers. He was responsible for meeting all timelines and budgets, assuring…

ID: 722568 Delaware, USA

Practical Application of GLP, GCP, and cGMP to Pharmaceutical, Device, and Biotechnology Firms

As Vice President at a pharmaceutical company, Expert formulated eight pharmaceuticals for use in their patented buccal delivery platform technology. Five formulations were acceptable to FDA and were allowed to proceed into human clinical trials under IND controls. Four of…

ID: 722432 Virginia, USA

Biotechnology Product Reviews, Biologics, Drugs & Medical Devices, FDA Litigation, Vaccines, etc.

Over 18 years experience with legal, scientific, business and regulatory issues affecting the research, development and commercialization of biomedical and information security products. Recognized expertise in strategy development, audit and due diligence, outsourcing, and FDA regulatory matters, including consulting for…

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