Hello everyone
I am a SD/MM consultant and have worked for manufacturing & professional services companies in my career.
Currently I have been selected to work on a project for a pharma company and I have some basic doubts:
- I know that pharma companies have to follow certain compliance/regulations.
Does this impact/modify the standard SAP SD OTC and MM P2P Business processes ? (In short - how are these 2 processes different from an SAP implementation for a manufacturing company).
- Our client has mentioned that - prior experience of a pharma company is preferred.
Hence I want to know "what regulations/compliance information or any other important information knowledge is expected from a SAP SD/MM consultant"
I want to get as much information as possible before being deployed at a pharma client.
Hence I require some input from you guys.
Please let me know your thoughts.
Thanks for your time.
- Vin