狠狠撸shows by User: praveenmoparthy1 / http://www.slideshare.net/images/logo.gif 狠狠撸shows by User: praveenmoparthy1 / 狠狠撸Share feed for 狠狠撸shows by User: praveenmoparthy1 https://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...