Online Free Career Talk by Relejuvant @ 11th January 2018
Source Data
Bioavailability
What is CTCAE
Merry Christmas
Merry Christmas
walk-in interview in Advantmed India LLP for B.Pharm/ M.Pharm/B.Sc /M.Sc candidates
Vulnerable subjects
What is Investigator's Brochure
Comparator in Clinical Research
How many codes are present in Nuremberg's code
Data Clarification Form (DCF)
Designing in Phase I trial
What is the next step after Data Validation in CDM
Primary end points in a Trial
What is the next step after Data Collection ?
Designing scientifically sound protocol in Clinical Trial
Protocol is a pivotal document for
conducting a clinical trial. All the different steps that would be implemented
and executed in a clinical trial have to be clearly documented in protocol.
Generally the sponsor of a clinical trial would draft the protocol. Once a protocol is drafted
initially it undergoes different corrections and modifications before deciding the
final version. But drafting and finalizing a clinical study protocol is not
sufficient to start a clinical trial.
Before
starting a clinical trial the protocol along with other important documents
like Informed consent form (ICF), case report form (CRF) has to be sent to the regulatory
authorities for approval. The regulatory authorities in different countries
would check the proposed protocol thoroughly with special emphasis on the
safety, well being of the subjects. If the design of the study in the protocol
and well as the methodologies that is depicted in protocol, reflects that trail
subjects safety is maintained, then the protocol gets approved. Designing a
scientifically strong protocol is one of the most important step in any clinical
trial.
Unexpected Adverse Drug Reaction
Walk in Interview in Dr.Reddy's
Quality Control (QC)
Quality Assurance (QA)
Full form of CRF
Different types of Database lock
Different types of Database lock
Non-inferiority trial
Electronic standard comes under which ICH topic?
Genetic Susceptibility
Happy Dussehra
Non-Inferiority trials
Benefit vs risk ratio in Clinical Research
Full form of DCF
Job opportunity in Inventive Health Clinical
Full form of CTCAE
Program Data Vector (PDV)
Principles of Belmont Report
In which year Nuremberg code was published
Please Contact-http://www.relejuvant.com/
Phone: 9550104680
Email: contact@relejuvant.com
Kondapur
Hyderabad – 84
Full form of ICF
Full form of IEC
Full form of IND
Causality assessment in Pharmacovigilance
Bioavailability
Subject Identification Code
Dose Ranging Study
Protocol
Clinical Data Management Career
What is the first section of ICH-GCP
Benefit vs Risk ratio
Single Blinded Study
Causal Relationship
PEM
Full form of GLP
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