Sessions running from April till June 2020
Attend or send your staff to our QA and GMP short course training sessions for up-skilling, professional development and to enhance the performance of your business.
SEERPHARMA TRAINING HAS GONE VIRTUAL
Live, interactive, instructor-led group training
The COVID-19 pandemic demands innovative solutions. As the pharmaceutical, medical device and life science industries grapple with unprecedented challenges, SeerPharma has adapted its training sessions from a classroom to a virtual environment to help you maintain business continuity.
SeerPharma is excited to bring you the following schedule of virtual-classroom QA and GMP training courses for the remainder of 2020.
HOW WILL IT WORK?
Physical distancing…not social distancing
Training programs are adapted for delivery in an online virtual-classroom.
Participants will be provided with a PDF of the training material in advance of the training should they wish to print and annotate notes. Participants will be connected to the trainer and other participants via online collaboration tool Zoom with connected video (webcam / screen sharing) and audio (computer audio or phone dial-in). Theory will be delivered by the trainer sharing their screen of the PowerPoint presentation. Facilitated workshops will be run in digital breakout rooms (e.g. a group of 12 might split into 4 breakout rooms each with 3 participants to separately work on a problem). Breakout rooms can call the trainer in for support when required and the trainer can electronically bring everyone back to the main session to debrief when appropriate.
A one-day course in the classroom will now be run over two days as 2 x 3.5 hour sessions. Each 3.5 hour session will include a break.
WHAT WILL I NEED?
Participant needs are very basic. You will need a computer with a good internet connection and preferably a headset (headphones with microphone) but alternatively you can dial-in via phone line.
SCHEDULE
The following courses are scheduled for delivery in the next 3 months. Click a course title for more information and registration details.
| Courses | Dates |
| Release for Supply | 8th and 9th April 2020 |
| Process Risk Assessment | 5th and 6th May 2020 |
| Validation (2 days) | 11th, 12th, 13th and 14th May 2020 |
| Root Cause Analysis and CAPA | 9th and 10th June 2020 |
