| » | Drug Regulatory Affairs Executive : Responsible for preparing, Submitting applications for CDSCO, Responsible for preparing, submitting applications for cGMP, GMP & GLP. (1627 views ) |
| » | Drug Safety Associate : Having basic knowledge on ARISg, Search for literature tittles with abstract from EMBASE (1504 views ) |
| » | Drug Safety Associate : Single ICSR processing, Can process all clinical, spontaneous, non interventional and Legal cases, Basics of pharmacovigilannce. (1559 views ) |
| » | Drug Regulatory Affairs Executive : Preparation/Review of Annotated Comparison, Knowledge of PDF properties, Coordination with other departments like ADL, FD, QA, Plant & Project Managements for various regulatory documents required for dossier submission. (3327 views ) |
| » | Regulatory Manager : Communicating with global marketing persons & technical consultant to resolved the issue piled up during the Process of new & renewal marketing authorization & preparation of documents. - Resolve NOD raised by concerned regulatory agency up to satisfaction (2507 views ) |
| » | Regulatory Affairs Executive : Research and Development, Analytical Basic, Method Validation, Method Development, And Other Processing Involved, Handling LCMS System. (3029 views ) |
| » | Drug Regulatory Affairs Executive : Responsible for preparing, submitting applications for CDSCO, Responsible for preparing, submitting applications for cGMP, GMP & GLP. (1795 views ) |
| » | Drug Safety Associate : Medical coding using MedDRA and WHO-DD, Case processing including data entryand narrative writing for PMS, CT andliterature cases, Ensure all medically relevant information is transcribed from source documents into the safety database (1784 views ) |
| » | Drug Regulatory Affairs : QA, IPQA, Regulatory Document Review, Calibration of IPQC equipment’s and instruments as per schedule, Perform Line clearance activity at various stage of manufacturing and packing. (2656 views ) |
| » | Regulatory Affairs Executive : Evaluation of Binding Efficacy of starch isolated from Dioscorea fluribenda, Microemulsion-A Versatile Dimension of Novel Drug Delivery System (2996 views ) |
| » | Regulatory Affairs Manager : Comprehensive knowledge of medical writing and analyzing complex medical data,Knowledge of e-learning and publication development (3232 views ) |
| » | Pharmacovigilance Executive : Reporting of the Adverse Drug Reactions, Updation and Maintenance of Pharmacovigilance Master File, Preparation and maintenance of Safety data Exchange Agreements (2378 views ) |
| » | Drug Safety Associate : Accountable for handling ICSRs received via data exchange systems, disposition of valid items into ARIS from IRT for further processing in ARIS. (3686 views ) |
| » | Regulatory Affairs Executive : To be involved with all registration related tasks, Post Approval Authorization Variations, Renewals, Receipt, preparation and submission of all applicable updates, amendments, resolutions and any other correspondence required by regulatory authority (4397 views ) |
| » | Fresher Drug Regulatory Affairs Executive : Responsible for conducting assay, Related Substances tests, Handling and performing calibration of analytical instruments, UV Spetrophotometric Method Development and Validation for Determination of Lacidipine in Pharmaceutical dosage form. (3070 views ) |
| » | Fresher Drug Regulatory Affairs Executive : Early stages of Drug Discovery, Development and Approval process for Global Regulatory Market, Knowledge on US FDA, EMA, ICH, WHO, OECD guidelines, Dossier compilation and submission of DMF, ASMF, ANDA, IND, CTA, NDA, MAA, to various regulatory authorities across the world. (3821 views ) |
| » | Fresher Regulatory Affairs Executive : Clinical Research Methodology, Roles and responsibilities of involves in clinical research, Ethics and Regulations in Clinical Research, Case Report Form design, Clinical data management, Regulatory affairs. (2951 views ) |
| » | Fresher Drug Regulatory Affairs Executive : Preformulation, Formulation and development, RnD, Technology Transfer, Production department, Formulation and Optimization of Chronomodulated Press Coated pulsatile drug delivery system of Carvedilol. (3110 views ) |
| » | Fresher Drug Regulatory Affairs Executive : Formulation and Development (R & D), Production, Regulatory Affairs, Glatt Coater, Pan Coating Machine, Spray Dryer, Rapid Mixer Grinder, Planetary Mixer, Dissolution Apparatus, Disintegration Tester, Friability Tester, Blender, Direct Compression, Orbiter Shaker, Ph Meter, Extruder Spheronizer, Etc. (3163 views ) |
|