狠狠撸shows by User: praveenmoparthy1
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狠狠撸Share feed for 狠狠撸shows by User: praveenmoparthy1https://cdn.slidesharecdn.com/profile-photo-praveenmoparthy1-48x48.jpg?cb=1595233705鈥� ICH, GCP, USFDA & GAMP Guidelines.
鈥� Principles of Pharmacology & Drug Discovery & Development.
鈥� Good knowledge on Validation and Chromatography.
鈥� Essential Documentation filling & maintenance in Clinical Research & Regulatory Submissions.
鈥� Informed Consent process, enrollment, Case reports, Study reports, Source documents.
鈥� IEC / IRB submission or notification procedure for approval of Study Procedure.
鈥� 21 CFR Part 11.
鈥� E2A Guidelines.
鈥� Demonstrated proficiency in composing written communications.
鈥� Excellent Interpersonal skills to behave in a best possible ways with the visitors in the company.
鈥� Proficient in the use of Microsoft Windows and Office software, a calculator and...