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adventitious agents
0:14:53
A sensitive sample preparation pipeline for adventitious virus detection using nanopore sequencing
0:08:47
Safety Evaluation & Toxicology ASR Review Video 2022
0:53:46
Validating and implementing nucleic acid testing-based methods for mycoplasma detection
1:07:14
VIRAL SAFETY BY DESIGN FOR CELL AND GENE THERAPY PRODUCTS
0:02:21
Inside the KappaMab manufacturing process
0:02:11
Viral vector production series: Keeping up with regulatory demands
0:20:19
15-minute Webcast: Assessing Viral Clearance in Early Phase Process Development
0:56:46
[Quality] ICH Q5A
0:45:06
Fermentative production of enzymes-amylase and protease
0:00:21
Seed Germination Stage 1 vs Stage 7
0:18:06
Serge Ohreser| Merck Millipore | France | Vaccines 2014 | OMICS International
0:04:15
Step 8: How to do IND Life Cycle Management? | Regulatory Learnings| DRA
0:02:56
Introduction to Viral Safety Part 1 - Two Minute Tuesday Technical Training
0:01:14
Risk factors in the development of stem cell therapy | RTCL.TV
0:01:09
Risk factors in the development of stem cell therapy | RTCL.TV
0:03:44
ABRF2024: Optimizing Core Communication and Collaboration with Veterinary Staff
0:17:53
1.5. Генная терапия: формуляция, валидация производства, стабильность, посторонние агенты
1:05:15
Cell and Gene Therapy Solutions: Enabling PSC Translation Workflows
0:02:15
Step 6: How does USFDA review an Investigational New Drug (IND) application? | Regulatory Learnings
0:15:24
Drug Device Combination Products | Episode 01- What are the Regulations for Combination Products?
0:04:42
Step 7: How are Clinical Trials Registered in USA? | Regulatory Learnings
0:24:37
Episode 27: MicroQuant™- Modernizing Quality Control Testing
0:05:30
Orphan Drug Development | Episode 07 - How to get Orphan Drug Designation in Japan | MHLW | DRA
0:05:30
What is Investigational New Drug (IND) Application? | Regulatory Learnings | Drug Regulatory Affairs
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