Bringing Direction
to a Very Indirect Process
Pharmaceuticals
Biotechnology
Medical Devices
Dietary Supplements
Our clinical supply chain wasn’t able to keep up with our expanding clinical program putting the addition of several countries at risk. Jeiven’s expertise brought our contractors in-line and our study completed enrollment on time.
Anonymous • VP, Clinical Operations
Developing new products is complicated. Jeiven helps keep your processes moving in the right direction.
Jeiven brings over thirty years of experience to the goal of providing pharmaceutical, biotech, medical device, and dietary supplement companies, government agencies and universities with an unparalleled level of service and dedication to ensure the success of their projects.
We provide GMP, GCP, GLP, GDP and DEA consulting, auditing and training services globally. We also provide Regulatory, Quality and Clinical Supplies consulting.
We take pride in providing, above all else, Reliable Guidance to clients of all sizes.
Industries We Serve
Jeiven can make sure you are up-to-date on the latest standards and regulations.
In addition to our regularly scheduled courses, Jeiven can provide customized on-site training to your team at your site.
Featured Seminars
DEA: Controlled Drug Substances Training
Join us online for an informative and interactive day of DEA training. Our experts will guide you through DEA regulations and answer all of your DEA-related questions.
NEXT SESSION:
OCTOBER 15 & 16, 2024
11AM-3:00PM ET each day
Clinical Supplies Training: The Basics and Beyond
Join us for an on-line exciting five-day course which will focus on the fundamentals and select advanced topics of the clinical supplies process.
2024 Schedule:
September 23, 25, 27 and October 1 & 3, 2024
10am – 2pm ET each day
Clinical Supplies Training – Blueprints for Complex and International Challenges
Have you been looking for a course to delve into more advanced Clinical Supply topics? Join us for an exciting two-day course.
2022 SCHEDULE:
Rescheduling in process. Contact us to be added to our email announcements list or for more information.
Site Glossary
- 222 Order Form
- 505(b)(1)
- 505(b)(2)
- 505(j)
- 510(k)
- Active Moiety
- ANADA
- ANDA
- API
- ARCOS
- Audit
- Biobatch
- Biosimilar
- BLA
- CAPA
- Clinical Study
- Clinical Supplies Management
- CMC
- CMO
- COA
- Comparator Drug
- CSOS
- DEA
- Due diligence
- FDA Form 483
- FDA Warning Letter
- GCP
- GDP
- GLP
- GMP
- ICH
- IND
- IRT
- ISO
- KYC
- Listed Chemicals
- MHRA
- NCE
- NDA
- PAI
- PMA
- QSR
- Quality Assurance
- Regulatory Compliance
- SOM
- SOP
- Substantially Equivalent
- YERS