Upcoming conferences about Pharmaceutical

Pharmaceutical outsourcing is growing exponentially amidst challenging price restrictions, US health care reforms and reduced revenues.

By : World Trade Group

Navigating Global Regulations and Reporting Requirements to Build Proactive Risk Management Strategies and Mitigate Potential Concerns

By : marcus evans

New directions in drug discovery and development

By : Health Network Communications

Europe’s largest and most influential early development/phase I congress which will address the critical issues in achieving seamless first in man studies.

By : Health Network Communications

This 90-minute webinar will help you understand the problems that can occur with statements by pharmaceutical manufacturers directed to off-label uses of pharmaceuticals.

By : Compliance online

Minimize your drug attrition rates by improving translation from preclinical to clinical development

By : Hanson Wade

Aiming to guarantee your excellence in deal making and expanding into today’s most attractive markets, we introduce to you our 6th Annual Licensing in Generics.

By : Fleming Europe

Leading provider of Oracle's clinical trial, data, and drug safety software will discuss a recent project for a top pharmaceutical company that entailed the merging of multiple drug safety systems.

By : BioPharm Systems

In this seminar, the application of the terms GLP and GMP will be explored, as there is often confusion in their application during development. This seminar will define the terms and their application in the development environment.

By : Compliance online

This ICH Q10 training /webinar will discuss the evolution and interpretation of the pharmaceutical GMPs as a quality control regulation to the Quality Assurance emphasis of the Pharmaceutical Quality System as defined in ICH Q10.

By : Compliance online

When orphan drugs are still at the stages of development, the latest and most accurate information is required for the drug to advance efficiently. Fleming Europe organizes the 2nd Annual Orphan Drug Congress 2012, where worldwide pharmaceutical experts will share their experiences and insight.

By : Fleming Europe

This webinar will help you understand how non-IND clinical trials at non-US locations can be used successfully to support an IND/IDE or a marketing approval application.

By : Compliance online

Progressive Business, Legal and Regulatory Strategies to Increase Your Market Share

By : The Canadian Institute

Now in its seventh year, the Global Pharma Manufacturing Summit has grown into the premier networking opportunity for industry leaders involved in small molecule and biologic pharma manufacturing.

By : World Trade Group

This webinar will help you establish an effective Good Clinical Practice (GCP) by providing a current, accurate and complete (CAC) review and applicable regulations for clinical trials or studies, the requirements and compliance in a systematic, integrative (SI) manner.

By : Compliance online

The seminar integrates both approaches to provide a comprehensive method to implement the systems.

By : compliance2go

The seminar integrates both approaches to provide a comprehensive method to implement the systems.

By : compliance2go

This FDA software validation Webinar/training will discuss how to self audit and ensure validation and software quality processes that will pass FDA inspection.

By : Compliance online

This seminar will discuss how to comply with FDA's ongoing Part 11 inspection program

By : Labcompliance

This webinar will highlight strategies to create a robust system of reporting and investigating deviations and other non-conforming events as part of an effective quality management system, as well as understand the regulatory requirements of corrective and preventive action system (CAPA)

By : compliance2go

To expedite the process of bringing a product to market through the 510(k) program, it is imperative the medical device makers understand the recent changes and be able to prepare a 510(k) using a CAC-SI method.

By : compliance2go

This webinar is intended to provide practical and actionable guidance on how to proactively prepare for a sustainable FDA Bioresearch Monitoring (BIMO) inspection and the proper response, if necessary, during and after the inspection including Do’s and Don’ts.

By : compliance2go

As industry has been looking to reduce costs, improve efficiency, the FDA has begun to more closely scrutinize the industry’s effort to make certain that the above mentioned controls are in place. In this effort the FDA is focusing on supplier control and sampling issues.

By : compliance2go

4th Vaccines China 2012 is timely and has been researched with the industry to provide the most comprehensive event focused on vaccines development through to manufacturing. Good manufacturing practices and strategies will be reviewed, alongside potential block-buster technologies and R&D projects.

By : IBC Asia (S) Pte Ltd

Join industry professionals at SMi's masterclass, Opinion Leader Development which is being led by The Central Group.

By : SMi Group Ltd

This meeting provides you with key insights into the drug safety challenges affecting you and gives you an excellent opportunity to discuss these diverse issues in a conference format.

By : Health Network Communications

This webinar on pharmaceutical water systems will explain practical best practices for outlet use and sampling to reflect the true water quality and how to most effectively use the resulting data to improve manufacturing’s water use practices.

By : Compliance online

Accel-Account Manager allows life sciences companies to easily and cost-effectively manage user accounts without technical knowledge.

By : BioPharm Systems

This 90-minute webinar on compliant foreign manufacturing facilities will help you understand the problems that can occur with foreign manufacturers of pharmaceuticals. Recent inspections and enforcement actions by FDA have brought the topic into greater focus.

By : Compliance online

PHARMATEC JAPAN is a new event dedicated to "Drug Packaging and Delivery Technology" for the pharmaceutical, biopharmaceutical, veterinary and medical industries in Japan

By : Businesswise Communications