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: 726401 New York, USA

Hydrogel Science and Technology for Drug Delivery, Medical Devices and Consumer Products

Expert’s major contributions are in microbial control of wide range of medical devices and pharmaceuticals. He has a background in chemical engineering and polymer science. He has decades of experience from numerous companies- large device and pharmaceutical companies to startups…

ID: 726392 Canada

Biostatistics Phase I, II trials, Translational research; Design, Analysis, Presentation

MD and MS in biostatistics with more than ten years of relevant professional, supervision and management experience • Experience in providing support to biomedical researchers regarding statistical aspects of study design • Expert in statistical techniques used in analysis of…

ID: 726340 Switzerland

Market Access and Riembursement of Orphan Drugs in Europe

Expert is a senior executive with expertise in International Market Access and Reibursement in Europe, UK, Canada and Australia. Expert has over 20 years experience in the pharmaceutical sector and played various roles within major Pharma/Biotech companies as well as…

ID: 726302 India

Product Development, Quality Assurance, GMP Audits, Qualifications, Troubleshooting, Pharmaceutical, Nutraceutical, Production Issues, GMP Compliance, Pharmaceutical Dosage Forms, Quality Control

Expert has more than 24 years of experience Internationally (New Zealand; Australia; Oman, and India) in pharmaceutical formulation plants, Product Development; Analytical development; Scale-up, Technology transfer; Manufacturing, Quality Assurance; quality control (testing and releasing); Lead regulatory audits and meet the…

ID: 726245 Minnesota, USA

Implantable and Non-Implantable Medical Device Risk, Safety, and Failures

He has experience in developing, writing, and submitting risk management related documentation to support Notified Body, 510k, PMA-S, and PMA submissions (Class I, II, and III). He has experience in the legal and safety requirements between 510k and PMA devices…

ID: 726229 United Kingdom

Pharmaceutical Licensing, Life Science Licensing, Commercialization

Expert has worked with a number of pharmaceutical and life science companies at senior level as either employee, consultant or interim manager, supporting initial public offerings and other fundraising activities and cross-border M&A. He has particular skills in due dilgence,…

ID: 726173 Texas, USA

Finance, Licensing, Life Sciences Investing, Business Development, General Management,

From its inception in 2003, Expert led a team of healthcare professionals to raise $325 million and manage a royalty-based private equity fund to acquire royalties from research institutes, inventors, and companies until his departure in 2009. Prior to 2003,…

ID: 726027 Maryland, USA

Industrial Hygiene, Non-Friable Asbestos-Containing Materials, Formaldehyde, Silica, Indoor Air Quality, Mold, Accident Investigation, Auditing and Hazard Assessment

He has conducted numerous indoor air quality and environmental mold assessments for commercial and residential environments. Assessment includes monitoring for applicable indoor air consituents, developing corrective action plans, and verification of correction/efficacy. He also lead the indoor air quality committee…

ID: 726016 New Jersey, USA

Biotech, Pharma and Medical Device Product and Process Development, Scale-up & Commercialization

His approach to process validation is that PV begins at the process development phase. A process that is well understood, well defined as per the critical to quality attributes with an understanding of the variable interactions prior to the definition…

ID: 726001 Netherlands

Regulatory Affairs and Pricing and Reimbursement-European and Emerging Market

She has advised many International clients with regards to requirements for dossiers as well as routemap for ANDA Procedure in addition to the requirements for DMF dossier as well as routemap for EDQM Certificate of Suitability Procedure. She has worked…

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