. Dealing with eCTD Submissions on Raaj GPRAC鈥檚 In-house demo software.
鈥� Awareness of Regulatory System of USFDA, Europe (EMA), RoW, ICH Guidelines.
鈥� Dossier preparation in CTD, ACTD Format, Electronic submissions (NeeS, eCTD).
鈥� Assisted in technical documentation, Workshop/seminar presentation while developing the Regulatory Affairs Consultancy business.
We鈥檝e updated our privacy policy so that we are compliant with changing global privacy regulations and to provide you with insight into the limited ways in which we use your data.
You can read the details below. By accepting, you agree to the updated privacy policy.
