Training
All good laboratory practice regulations require that personnel engaged in or supervising the conduct of a study have the education, training or job experience needed to perform their duties properly.
Organizations conducting non-clinical and veterinary clinical trials understand the importance of training, so much so that many have department/personnel dedicated to training. Due to the confidential nature of the studies and the specialized functions being performed, the required training is most often accomplished internally. On the occasions when external training is allowed and importantly, available, the cost of the training can be prohibitive, especially when training is only needed for a few individuals.
Consider how QAS can meet your training needs, in-house.
US and International Good Laboratory Practice Training
- 21 CFR Part 58 (FDA GLP)
- 40 CFR Parts 160 and 792 (EPA FIFRA and TSCA, respectively)
- OECD ENV/MC/CHEM (98)17
- Japanese MHLW Ordinance No. 21
Specialized Training including, but not limited to:
- New employee orientation or periodic refresher training
- Good documentation practices
- Regulatory and/or third-party inspection preparation
FDA CVM, EPA OPPTS, ICH and OECD guidelines - Pesticide product labeling
If you have the need for a specialized training program and do not see it listed in the choices above, please don’t hesitate to contact us. Where possible, we can tailor or develop a program to meet your specific needs.