Webinars

Webinar: Ensuring transparent reporting of clinical data with Medical Publication Professionals
Following CONSORT recommendations is of utmost importance to ensure transparency when reporting or publishing results of any randomized controlled trial (RCTs). Manuscripts involving a Medical Publication Professional showed improved adherence to CONSORT guidelines across Asia, Europe and North American journals.

Date: Jun 25th, 2015
Timing: 10.00 AM – 10.45 AM EDT

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Webinar: CDM Role in Late Phase / Safety Registries
Late phase trials, also called as Post Marketing Surveillance (PMS) Studies, are often observational where the effectiveness of a device/ drug is measured across the long duration of its exposure in general population. As late phase trials are becoming a necessity and a requirement by FDA, the role of CDM is also becoming challenging.

Date: Mar 25th, 2015
Timing: 10.00 AM – 10.45 AM EDT

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Webinar: Data Analytics to Support Fraud Detection
The success of any clinical trial depends on the accuracy and integrity of the study process and data produced from the trial. Detecting inadvertent errors and fraudulent data is paramount at every step.

Omission of critical data, reporting of only positive outcomes and none of the adverse outcomes, etc. are some instances which could have dire consequences on the overall study. Data analytics techniques have a significant role to play in the early warning, detection and monitoring of fraud.

Date: Dec 04, 2014
Timing: 10.00 AM – 10.45 AM EST

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Webinar: Conducting Clinical Trials for FMCG Sector - A Case Study
FMCG companies function in an environment of high competition and fickle customer loyalty with many brands touting their superiority. In such a scenario, the presence of empirical data to bolster a product claim can provide a company with a strategic advantage in the marketplace. As a result, 'claims studies' have become an important facet of a FMCG company's R&D spend.

Date: Aug 28, 2014
Timing: 10.00 AM – 10.45 AM GMT

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Webinar: Managing a Hybrid (Paper-EDC) Study - Challenges and Learning
The paper case report form (CRF) is a preferred way of data capture for small size or fast track studies. However, there are occasions where a hybrid study needs to be designed or a transition from paper to electronic data capture (EDC) is sought. Increase in number of patients and sites to real time monitoring of data, the reasons for this may vary.

Date: Jun 26, 2014
Timing: 10.00 AM – 10.45 AM EST

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Webinar: Defogging the Regulatory Scenario for Biological Products in India
In the past decade biopharmaceutical companies have focused on developing new biological products to treat medical conditions with high unmet needs. The commercial success of these drugs has also attracted several companies to make generic equivalents or 'biosimilars' of the aforementioned biological drugs.

Date: May 22, 2014
Timing: 10.00 AM – 10.45 AM EST

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Webinar: The impact of regulatory changes on drug safety reporting in clinical trials
Clinical research worldwide is a multi-billion dollar industry. India is an emerging destination for clinical research, but it is susceptible to the vagaries of regulatory winds.

Recent regulatory changes have greatly altered the methodology of drug safety reporting in clinical trials. To clear the air and bring some clarity to the stakeholders, we are organizing a webinar - The impact of regulatory changes on drug safety reporting in clinical trials.

Date: Jan 16, 2014
Timing: 10.00 AM – 10.45 AM EST

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Webinar: Defogging the Clinical Research Regulatory Scenario in India
The Indian regulatory scenario has witnessed unprecedented upheaval in the past few years. Touted as one of the fastest growing destinations for clinical research by analysts, India has a huge impact on the global clinical research trends. Biopharmaceutical companies from all across the world have shown growing interest in regulatory changes happening in India and its impact on their clinical research programs, which is gradually overshadowed by grave concern and uncertainty.

Date: Dec 12, 2013
Timing: 10.00 AM – 10.30 AM EDT

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Webinar: Publications & Medical Communications: Unexplored feature of Medical Writing
In last few decades, new information is continuously being added to the field of medicine in the form of research, clinical experience, new ideas or in response to increased scrutiny from regulators. All this information generated needs to be effectively communicated to different audiences, e.g. regulators, physicians, healthcare professionals either in the form of regulatory documents or publications and communications.

Date: Nov 14, 2013
Timing: 9.00 AM – 9.45 AM EDT

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Webinar: Clinical Data Management: A Strategic Intervention
Determine the appropriate outsourcing model for your business requirements in clinical data management. This session will help you gain perspectives on key parameters that influence outsourcing decisions and identify factors to consider when evaluating clinical data management outsourcing partner.

Date: July 18, 2013
Timing: 10 AM – 10.45 AM EDT

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Webinar: Off-Shore or Not to Off-Shore: Critical Factors Impacting Decision for Outsourcing Medical Writing
Take an informed decision on outsourcing/ off-shoring medical writing. This session will help you note critical factors that must be considered while outsourcing medical writing, help understand and mitigate the challenges faced offshore for guaranteed success.

Date: July 16, 2013
Timing: 10 AM – 10.45 AM EDT

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