New Indian Regulatory Guidance by Central Drugs Standard Control Organization Guidance for Industry on Submission of Clinical Trial Application for Evaluating Safety and Efficacy - Central Drugs Standard Control Organization...

Indian Clinical Data Management market is expected to ramp up to $150 million MNCs are more than willing to outsource their needs to India because of it\'s technological innovation, creditable quality, operational flexibility, cost effectiveness, time-to-market and competitive advantage according to Koteshwar Govind, Deputy Manager,...

India: Attractive Market for Biopharmaceutical Companies Looking to Accelerate Their Clinical Trials The Clinical Research Market in India is growing at a very rapid rate according to anyone’s statistics…It is exploding according to all the hype. ...

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Site Management » Site Coordination

Patient data scan and short-listing of patients for chronic diseases
Help the investigator in screening patients
Assisting investigators in the Informed Consent Process · Coordination and management of laboratory samples, courier and follow-ups of lab reports
Drug accountability and dispensing at the site
IVRS (Interactive Voice Response Services) for patient's randomization in randomized studies
Investigational product management, dispensing, temperature monitoring and accountability
Preparation, attendance and follow-up of monitoring
Completing CRF entry with minimal error (All Neeman CRCs are trained and certified to log both hardcopy CRF and eCRF)
Preparation, attendance and follow-up of Audit
Trial closeout: preparation, attendance and follow-up; forwarding the necessary information of closeout to clients

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