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: 730048 California, USA

Commercial and Industrial Elevator and Escalator Design, Development & Maintenance- Expert

Expert, is a nationally recognized Certified Forensic Litigation Consultant (FEWA) with over 50 years of industry experience and a court approved expert witness for over 22 years. His expertise with conveyance litigation successfully providing owners, carriers and attorneys knowledgeable and…

ID: 729549 California, USA

Pharmaceutical Quality Assurance, Quality Control, Supplier Selection and Supplier Quality

Expert has extensive expertise in GMP matters in the pharmaceutical and medical device industries. During his 20 years in industry, he devised, managed and led programs to assure compliance to drug GMPs, GLPs and GCPs. Key areas of expertise included…

ID: 729349 Michigan, USA

Life Science, Biotech, Pharmaceuticals: Research and Development, Smart Manufacturing/ Supply Chain, and Market Launch/ Commercialization

Expert has over 20 years of experience in strategic innovation, system building, and delivering value solutions for global markets. His focus is on building infrastructure synergies between science, technology, and finance. As a Strategic Advisor, he has experience with: •…

ID: 728655 United Kingdom

Process Safety, Risk Assessment/Management Major Accident Risks, Hazards and Land Use Planning

Process Safety has been the main focus of Expert's work as he seeks to assist companies avoid accidents completely (by eliminating hazardous materials or processes) or prevent them through providing protection (containment or control). In some circumstances the only available…

ID: 728425 California, USA

Designing and Implementing Quality Control Stability Programs, Authoring Stability Sections

Expert has over 10 years experience in the areas of QC Stability (Drug Product and API). In addition, Expert has many years of experience in drafting QC Stability sections for the following submissions for the FDA: IND, NDA, BLA, PAS,…

ID: 728193 California, USA

Medical Devices

Expert is a medical device consultant and executive with more than 20 years experience in the medical device industry. His expertise spans all aspects of medical device commercialization, from medical device product development to medical device manufacturing and quality control;…

ID: 727252 New York, USA

Internal Controls Remediation, SOX and FCPA Compliance, Risk Management, Financial Due Diligence

Expert S. Expert, CPA is an audit partner with a New York full-service accounting firm specializing in audit of pubic companies, internal controls and SOX compliance, due diligence, and risk management. Expert has more than 20 years of public and…

ID: 726912 North Carolina, USA

Pens and Markers for the Stationery and Cosmetic Industry, Specializing in Fluid Delivery Systems.

Expert has been active in product development for the stationery and cosmetic industry for 30+ years. Pens that he has contributed in a major way, have been sold worldwide and in very large quantity for customers as varied as Hewlett…

ID: 726165 Venezuela

Asset Care and WCM: Maintenance, Reliability, SH&E, STR, Supply Chain for Maintenance, EAM/CMMS.

- He has applied his maintenance management background as functional developer, trainer, and project director for EAM/CMMS multi-site implementations for several industries. - It includes participation from the organization of maintenance warehouse until maintenance process automation resulting in successful implementation…

ID: 725858 India

Regulatory Affairs, Technology Management, Pharmaceutical Industry, Turnaround Management

Expert has experience in applying 21 CFR Part 11 to the manufacturing of pharmaceuticals and preparing and facing FDA inspections. He has more than 20 years of experience in various facets of API industry ranging from research to manufacturing, projects,…

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