regulatory affairs as a career path
TRANSCRIPT
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Plamena Entcheva-Dimitrov, PhD, RAC On-line Course
www.PreferredRegulatoryConsulting.com
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The Preferred Regulatory Consulting content in this presentation is copyright protected under United States law and applicable international copyright laws.
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Why Regulatory? What do we do? What is the growth potential? What are the necessary skills? What do you need to know and where do you
learn it?
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High impact on the company Interactive Stimulating See all – do all Sense of accomplishment
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Study, interpret and apply the regulations Advise the company on newly published or on
upcoming changes to existing laws/regulations / standards
Work with R&D on product development – follow regulations from product’s inception
Prepare submissions to regulatory agencies Involved in the clinical trial design and conduct Standard Operating Procedures Continuously train the organization on
regulations/guidances/directives/standards Safety reporting pre- and post-market Involved in product recalls
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Regulatory Product Development
Engineering Clinical
Non-clinical
Process Development Chemistry
Reimbursement
IP Lawyer Quality
Assurance
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The sky is the limit!!!
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Individual contributor Management track Expand into Clinical Affairs,
Quality Assurance or both
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morning
noon
evening
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PhDs MDs/PharmDs Lawyers MBAs Engineers MS Chemists
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Analytical Critical thinker “Roll up your sleeves and get the job done”
approach “Can do” attitude Creative Team player/excellent interpersonal skills Integrity Detailed oriented Excellent writing skills Mentor/educator
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FDA responsibility, authority, jurisdiction and structure: Inspections Warning letters Recalls Suspension / withdrawal of approvals Seizure Injunctions Civil and criminal penalties
EU Directives, Regulations Health Canada Australian Therapeutic Goods Administration (TGA) Many other emerging markets (e.g. Brazil, China,
India)
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• Food, Drug and Cosmetics Act of 1938 • Medical Device Amendments of 1976 • The Food and Drug Administration
Safety and Innovation Act (FDASIA) of 2012
Laws
Center Specific Guidance Documents
Regulations: Code of Federal Regulations
Title 21
• Good Laboratory Practices • Conduct of Human Research • Labeling Requirements • Recalls • Safety Reporting • Facility Registration • Audits / 483s
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Directives
Standards (ISO, IEC)
Guidances (MEDDEVs)
Consensus statements
Interpretative documents
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MEDICAL DEVICES DRUGS / BIOLOGICS
I. Quality Systems Regulations II. 21 CFR 807 and 814 for
submission content and format: 510(k), de novo, PMA, HDE
III. IDE for clinical studies IV. Design Control Concept V. EU Medical Device Directives
VI. ISO Standards VII. Complaint handling and
vigilance reporting
I. GMPs II. 21 CFR 314 for submission
content and format : NDA, BLA
III. IND for clinical studies IV. Quality by Design V. EMA – EU legislations and
regulations VI. ICH Guidelines VII. Vigilance reports
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On-line courses Universities Social networking, e.g. LinkedIn The regulators
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Networking, networking, networking Find a mentor
Open-minded Positive attitude Self-educate
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You have completed a 30-minute regulatory affairs on-line training
You can print this page for your records
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™
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