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At FDAQRC we partner your needs with the ideal Consultant. We have over 300 Consultants in our network to ensure we meet your technical requirements. Tell us about yourself and your needs in five easy clicks using the search feature below. You will be rewarded with short bio-sketches of potential Consultants for your project within 30 seconds.

If you are looking for a variety of services across locations or you’d rather speak in person; no worries, contact us as we are always keen to speak with you about your needs. Info@fdaqrc.com

About You
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Preferred Method:   Email   Phone
Best Time:   AM   PM   Evening   Anytime
About Your Needs
Service Type: First choose a category from the three presented. Each category reveals additional service types, be sure to check the relevant category to document all competencies. Note: If you uncheck a category box any data entered will be lost. You may search within all categories but only one service type at a time. You may search as multiple times.  *

 Audit/Compliance focused

 Regulatory or Medical Writing focused

 Technical Pharmacovigilance (PV) focused

 
 
 Acting as an Expert Witness
 Agency Guidance and Remediation
 Compliance Risk Evaluation
 Field/Crops
 Food and Supplements
 GcLP/ CLIA Clinical Laboratories
 GCP Investigator Site Audit
 GCP Phase I
 GCP Trial Master File
 GLP Animal Facility
 GLP Non-Clinical Laboratories
 GMP Biologics/Vaccine
 GMP Device Facility
 GMP Drug Facility
 GxP Computerized Systems
 GxP Document – clarify as CSR, NDA, TLFGs, Dossiers, IB
 GxP Mock Inspection
 GxP Quality Management System Gap Analysis
 GxP Training
 GxP Vendor (that is not a specified in this list)
 Independent Consulting
 ISO Implementation
 Post-Marketing Pharmacovigilance
 Pre-Marketing Pharmacovigilance
 REMS and Post-Authorization Studies Auditing
 Sponsor-level Inspections
 Submissions
 Veterinary
 Agency Interactions/Meetings
 Aggregate Reporting Creation/Review
 Clinical Evaluation Report Creation/Review
 Design Dossier Creation/Review
 External Patient Materials Creation/Review
 Human Factors Engineering Creation/Review
 IND Creation/Review
 Label Creation/Review
 NDA Creation/Review
 Periodic Reporting Creation/Review
 REMS and Post-Authorization Study Creation/Review
 Risk Assessment and Management Creation/Review
 Strategic Advice and Planning
 Submission Preparation/Review
 Technical File Creation/Review
 Aggregate Safety Reporting Creation/Review
 Literature Searching
 Medical Information Computerized Systems Implementation/Review
 Post-Approval Reaction Processing/Reporting
 Pre-Approval Safety Case Processing
 PV Master File Compilation/Review
 PV Risk Management Creation/Review
 REMS and Post-Authorization Studies Creation/Review
 Signal Management and Monitoring Activities
Other  
Location: *
Timeframe: *

e.g., Feb 2024 or 3Q 2024

Would you say the service request is "for-cause"?     Yes     No

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 BA    BS    BSN    DVM  
 MA    MBA    MD    MPH    MS  
 PharmD    PhD    RN  
  I am interested in short-term dedicated Consultant.
  I am interested in long-term dedicated Consultant.
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