Experts in Biotechnology

Top 7 experts
Osama Ibrahim
Osama Ibrahim

Gurnee, IL | Consultant Biotechnology

Dr. Osama Ibrahim is a highly-experienced Principal Research Scientist with particular expertise in the field of microbiology, molecular biology, food safety, and bioprocessing for both pharmaceutical and food ingredients. He is knowledgeable in microbial screening /culture improvement; molecular biology and fermentation research for antibiotics, enzymes, therapeutic proteins, organic acids and food flavors, biochemistry for metabolic pathways , enzymes kinetics, enzymes immobilization, bioconversion, and analytical biochemistry. Dr. Ibrahim was external research liaison for... Read more
Elliott Block
Elliott Block

Boca Raton, FL | 4 Decades Experience in Public/Private Biotechnology and Clinical & OTC Diagnostics

Senior results-oriented executive experienced in negotiation of licensing and joint ventures, business development, general management, P&L, operations. Track record in motivating and coordinating diverse resources to generate growth in technology-based companies. Strengths are evaluation, planning & direction of complex projects, including integration/motivation of all departments. Seeking to serve on 1) Board of Directors of public/private companies, 2) advisory boards, &/or 3) interim management.... Read more
Brett Vengroff
Brett Vengroff

Cambridge, MA | GCP, GLP, cGMP Compliance Training and Quality Assurance Audit Consultant at ComplianceLogix

Co-founder and Principal Consultant at ComplianceLogix, with over fifteen years of experience in the biopharmaceutical industry. Provides quality assurance audit and compliance training. Successfully established and maintained quality assurance systems worldwide, designed and improved business process workflows, training programs, and performance management systems. Specialties: Quality audit, vendor audits, clinical investigator audits, CMO audits, CRO audits, compliance training, online training, regulatory compliance, business process improvement, organizational alignment,... Read more
David DuRocher
David DuRocher

Chesnee, SC | Senior Vice President at Du All Controls, LLC

Qualifications Over thirty years experience in the pharmaceutical / medical device industry. Results-oriented individual with a track record of instituting and maintaining high levels of Quality Assurance, and leadership in the pharmaceutical, medical devices and biological industries. Expert in compliance, auditing, investigations, product complaint, validation, SOP development and assessment, PDMA, cGMP, CFR 21 related items, document control, State and Government regulations. 17 years Government Regulations, inspections, SOP Development. Individual has a minimum of 17 years... Read more
John Greenbaum
John Greenbaum

Orlando, FL | Owner, GDCI Consulting, Inc.

18 years of successful Regulatory Consulting and operating a Clinical Research Organization. Hundreds of therapeutic and diagnostic products have been brought to market with our help. We have substantial experience with regulators in multiple disciplines and generally good relationships with them. We work with virtually all branches and divisions of the US FDA. In Clinical Research we have ongoing trials at 11 institutions and support numerous others with clients research and clinical teams. Specialties: Regulatory Strategy, Regulatory Submissions, Regulatory approvals, Clinical... Read more
Martin Gollery
Martin Gollery

Incline Village, NV | Bioinformatics Consultant | Author

How can I help you? I am booked solid, but will give advice if I can help. If you would like to see what I am working on right now, check out the BioDatomics and if you are interested in joining with this community, let me know! I will be holding regular training and familiarization sessions online. Just setting up the plans now, so if you are already using biodt, let me know what you want to see in terms of NGS workflows, RNA-Seq, alignment tools, or Hadoop training videos. I am a genomics 'Big Data' kind of guy. I am known for being a technical guy that can talk to normal... Read more
Susan Caldwell
Susan Caldwell

Seattle, WA | Expert Regulatory Medical Writer

Background in regulatory medical writing (MW) and drug product development, with a strong publication record—an unusual combination of MW expertise, analytical skills, management experience, medical knowledge. Experienced in all phases of drug, biologic, and medical device products: • ICH-compliant regulatory submissions (INDs, NDAs, sNDAs, BLAs, sBLAs, 6 eCTDs, and 2 combination drug/device submissions), clinical study protocols, amendments, clinical study reports (CSRs), serious adverse event (SAE) narratives, investigator brochures (IBs), process development/CMC documents,... Read more