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.

×

Expert Directory

 

Having an expert witness or consultant at your side can help you navigate complex situations with confidence. These professionals understand your industry and excel at conveying crucial information, whether in a courtroom or a consulting environment. At Intellex, we have experts in over 30,000 areas in our database. We enable you to partner with an individual who has the knowledge, educational background, and relevant experience to support your needs effectively.

Utilize our expert finder tool to handpick the ideal mentor or consultant for your specific application.

ID: 728599 Pennsylvania, USA

DEA Compliance

In January 2009, Expert founded Employer as a compliance consulting firm specializing in federal laws and regulations relating to manufacturing and distribution of pharmaceutical controlled substances and regulated chemicals that are enforced by the Drug Enforcement Administration (DEA) through the…

ID: 728217 Maryland, USA

QC/QA, Sterility Assurance, Aseptic, Pharmaceutical, Biotech, Device Manufacturing & Testing

Environmental Monitoring Operations, EM Trends Reports, EM Remediation and Investigation. Cleanroom Contamination Control Practices, Behaviors, Personnel, Gowning, Cleanroom Traffic Guidelines, Process/Personnel and Product Flows. Microbiology Release Testing-Bioburden, Sterility Test, Growth Promotion, Materials Control, Microbial Identification, Bacteria Endotoxin, Biological Indicators Testing,…

ID: 727750 Canada

Regulatory Sub. NDS, ANDS, SANDS, NC, Cross References, Natural Health Products, Medical Devices

Expert's firm has extensive expertise in regulatory submission. They provide different regulatory strategies to their customer’s and prepare all types of submissions on their behalf. Expert also has extensive expertise in Narcotic’s regulations. Moreover, her firm has extensive experience in…

ID: 726908 New Jersey, USA

Drug and Vaccine Adverse Effects, Standard of Care, Hepatitis

Expert is board certified in internal medicine with a focus on biomedical clinical research. He received his PhD in immunology and medical genetics from the Department of Microbiology at UCLA in 1977. He also received his MD from UCLA in…

ID: 726226 South Carolina, USA

OSHA Compliance, Safety Engineering, Accident Investigation (Workers\’ Comp, etc.) and Environmental Remediation/Investigations

Upon graduation from the U.S. Merchant Marine Academy Expert served time in the U.S. Navy as Engineering Officer aboard a destroyer and continued on active reserve status for eight (8) years. Subsequently he received a Master of Science degree in…

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: 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…

ID: 725868 Montana, USA

Quality Assurance, Regulatory Affairs, Marketing and Business Strategy for Life Sciences Industry

He has performed compliance audits to 21 CFR Part 11. He has developed qualification protocols to test systems compliant with 21 CFR Part 11. He has developed advertising campaigns, written copy for advertisements and managed the creative development of advertisements.…

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,…

ID: 725380 Missouri, USA

Pharmaceutical Grade Medication, Medical Sciences and Medical Subspecialties

He has worked extensively with Alpha2 pharmacologic agents. His experience was acquired while being a medical director at Pfizer Pharmaceuticals. He is board certified in Sleep disorder medicine. He is board certified expert in pulmonary disorders. He is quadruple board…

Dev Tool:

Request: experts/pharmaceutical-regulations/page/4
Matched Rewrite Rule: ^experts\/([^\/]*)\/?([^\/]*)\/?page\/([0-9]{1,})\/?
Matched Rewrite Query: pagename=experts&searchKeyword=pharmaceutical-regulations&searchDiscipline=&paged=4
Loaded Template: page-experts.php