GMP Resources
All billing and milestones information is provided via the iLAB system. Cliens are required to register for an iLAB account to request production.
iLab: https://nch.corefacilities.org/account/signup/19
| 1Requirements |
Research/Development |
TOX / Large Research Production Requirements | GMP-Clinical |
|---|---|---|---|
|
Formal Project Request |
√ |
√ |
√ |
|
CDA |
√ |
√ |
√ |
|
iLABs Registration |
√* |
√ |
√ |
|
MTA |
As required |
√* |
|
|
Yield Assessment |
|
As required |
√ |
|
LPA |
|
|
√ |
|
Quality Agreement |
|
|
√ |
|
IPS |
|
|
√* |
|
RPP_MPP Informatoin |
|
√ |
√ |
1 Review the requirements description from the documents section below
*At this point, a cue will be booked for possible production date. It still depends on when Primers/Probes, Plasmids and Plasmid maps are received to start production.There are different services provided for each production.