Clinical Research Services classes near me in Kphb Police Station, Hyderabad

I am a clinical data management experienced person and I can give online tuition on any day. I have master degree in pharmacy. My skills are EDC management, clinical data management, clinical trial, risk management, TMF, medidata Rave, Inform. I can provide tution on Clinical trial, clinical Data management, ICH principles, Clinical Monitoring.

I am a teacher , I can give proper training of CDM course , and also will give proper guidance for your career growth. Attend the demo class and take the right decision.

I am an Indian clinical research professional in United kingdom.I did my Doctor of pharmacy (Pharmd) in India and Masters in pharmacology and drug discovery in UK.Im having 8 years of clinical research operations experience in India and UK.And i have been teaching clinical research classes both in India and united kingdom since 2019.

I am Pharm.D graduate from K.L.R pharmacy college in 2018. I had experience as associate professor for 3 years. I also worked as Safety associate at Iqvia.

I am a Sr Safety specialist, providing online training for pharmacovigilance and placement assistance after completing a course. End-to-end training will be provided along with real-time training.

im a pharmacist im about to learn clinical data management and I want to join clinical data management and switch my career to clinical research side

My Self Mohan Murali Gonnuri. I Completed my graduation on Bachelor of Pharmacy in 2022 with 75% I am looking for entry level opportunity in Life Sciences and Clinical Departments. I do have knowledge on Clinical Research, Pharmacovigilance, Clinical Data Management, Medical Writing, Medical Devices & Regulatory Affairs. My Skills are Include: - Clinical Trails, Drug Development Process. - Pharmacovigilance – Case processing, duplicate search, SAE, AE, ADR & Narrative Writing. - Clinical Data Management – Study Start up, Study Conduct and Study Close out Activities, Query Management, SAE Reconciliation. - Medical Writing – Protocol, Clinical Study Report, CRF, Informed Consent Form. - Medical Devices – IFU, CER, Labelling, IVDR and MDR. - Regulatory Affairs – NDA, ANDA, Generic Drug and Branded Drug. My Strengths are Include: - Time Management - Quick Learner - Quality Oriented Employee I believe in Hard work and Continuous learning. Hoping that will hear from you soon in a positive manner.

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Course Covered:- 1. Interdiction to Pharmaceutical Industry , 2. What is Quality Control,3. What is current Good Laboratory Practices [cGMP], 4.What is current Good Manufacturing Practices [cGMP], 5. What is US-FDA,6.Volumetric Solutions Preparation and Standasation , 7. pH- meter Operation, 8. Melting Range[M.R]apparatus Operation, 9. K.F.Titrator Operation,10.Loss On Drying [LOD],11.Sulphate Ash, 12. Working Standard Analysis, 13.T.L.C [Thin Layer Chromatography],14.Paper Chromatography , 15.Ultra Violet-Visible Spectro photo Meter [U.V] Operation and Calibration, 16.FT-IR Instrument Operation and Calibration 17.Hard Ness Tester Operation, 18.Friability Tester Operation, 19.Dissintigration Test Operation, 20.Dissolution Test [Apparats-1, Apparats-2] Operation and Calibration, 21.What is STABILITY, 22.What is Method Development and Validation, 23.what is CHROMATOGRAPHY, 24.What is H.P.L. C and G.C, 25. H.P.L.C and G.C- Instrumentation, Operation, Calibration, Maintainance, Trouble shooting, System suitability, etc….26. Resume preparation, Mock Interview and Personality development. (course material + Certificate + 300 HR mail IDs) Eligibility: Fresher's / Experience with B.Sc./M.Sc./B.Pharm/M.Pharm/P.hd/B.E.Chemical Course material is provided from the institute. M.Pharmacy Projects:- 1. Analysis Projects:-(Project + All Q.C Instruments Training + Job Assistance for Merit Students) Fee – single drug Rs.6500/- only, Combination drugs Rs.8500/- only, For Analysis

I am a post graduate in pharmacology and toxicology from NIPER HYDERABAD, with a deep knowledge on pharmacology and other pharmacy subjects with passion of teaching.

I had 1 year and 2 months experience in Accenture, Bangalore. I worked as a medical services associate. The work is to process and evaluate serious adverse events to ensure patients safety with emphasis on timelines and quality