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Contact us

Regulatory Affairs Specialist

ra

Duration :

5 hour(s)

Skill level :

Regulatory

Language:

English

Final exam:

Yes

Certificate of Completion:

Yes

CEU / CPD Accreditation:

Yes

Certification:

Gain a recognized and traceable certificate after completing the course : 

All our certificates are unique, authentic, CPD/CEU accredited, and FDA 21 CFR PART 11 compliant. Certificates validity can be checked online through our certificate online checker.

Description :

Embark on an enlightening journey with our “Regulatory Affairs Specialist” training bundle. This meticulously curated selection of courses is tailored to empower professionals navigating the complex world of pharmaceutical regulatory compliance. Under the expert guidance of Dr. Jefferson, with her substantial experience, this bundle offers comprehensive insights into key regulatory domains.

This learning path is a deep dive into the critical aspects of regulatory affairs, from understanding the essentials of pharmaceutical regulatory affairs to mastering the intricacies of compliance inspections, external audits, and FDA 21 CFR Part 11 regulations.

Key benefits of this bundle include one-year access to the latest content, a unique and verifiable certification for each course completed, and a final certificate upon completion of the entire path.

This training bundle is ideal for both individual professionals and teams. Whether you’re a regulatory affairs manager, a quality assurance specialist, or a human resources professional responsible for the training and development of regulatory affairs personnel, this program is a convenient, cost-effective, and comprehensive solution.

Join us to transform your career in the ever-evolving realm of pharmaceutical regulation.

Courses Included :

Pharmaceutical Regulatory Affairs

2 hour(s)

Regulatory Compliance Inspections and External Audits

2 hour(s)

Introduction to FDA 21 CFR PART 11 Online Course

1 hour(s)

Your Expert :

Ellena Jefferson
Dr. Jefferson
Dr. Jefferson is a CAPA Manager. She serves as a Training and Quality Advisor with ICONIC plc, a global provider for consulting and outsource development in the pharmaceutical industry. She holds a Masters of Science in Research Administration, Magna Cum Laude from the University of Central Florida. Dr. Jefferson is a fixer who continuously strives for excellence as a way of life; not just as a job.
USD: United States (US) dollar ($) ^

$240

Buy now

  Large group ? Request a quote !

This course includes:
One-year access
Updated content every month
Certificate of completion

GxP-Training Benefits

  • Experts : We work with the world's top experts in GMP, GLP, GCP, GDP, regulatory affairs, QA and pharmacovigilance.
  • Validated : All our courses are CPD/CEU accredited and we deliver a unique, traceable and authentic certificate to each learner.
  • Self-paced : access 24/7 to the course during 12 months at your own rhythm.
  • Smooth Experience : Each course starts with a video and ends with an exam and a valid certificate.
  • Up-to-date : each course is updated on an annual basis to remain valid along the Regulatory Body recommendations.
  • Instant Purchase : one click to buy and immediate access. Get certified today.
  • LinkedIn compatible : get a valid certificate at the end of each training program and publish it on LinkedIn with a Unique and Secure Link to your registered certificate.
  • HR management : all course programs are available either individually or as a batch to HR managers in order to pilot employees Training, follow their progress and send reminders.
  • Procurement optimized : instant Purchase Order, Online payment and PDF Invoice.
  • LMS compliant : each course is a SCORM object that you can distribute through your corporate Learning Management System.

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About us

GxP Training is a service provided by Axeda SRL, a recognized leader in digital regulatory learning. Axeda specializes in compliance training and assessment solutions specifically designed for life sciences companies and professional training organizations.

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