This webinar will cover effective and efficient ways to transition from paper to electronic records in a regulated environment. It will address compliance issues, complexity in decision making and implications specific to the pharmaceutical industry.
How do you efficiently manage this daunting task of converting all legacy paper records to an useful format?
How do you effectively organize this archived data in an orderly manner so that information is not lost or difficult to locate?
This webinar will discuss proven and practical strategies to optimize the storage and organization of legacy information, paper as well as electronic. The speaker will highlight effective methods to index and organize records and integrate them so that it is easy to retrieve information. A transition from paper to electronic records will involve a myriad of challenging and complex decisions that are to be made. Attending this webinar will equip you with the necessary information and know-how to ensure that you make the right decisions.
Why Should You Attend:
The tendency, after a drug fails in clinical trials, is to retain all related information permanently. There are vast stores of pre-clinical, clinical and drug safety paper records that are archived in many companies for drugs that failed to reach the marketing stage for a variety of reasons.How do you efficiently manage this daunting task of converting all legacy paper records to an useful format?
How do you effectively organize this archived data in an orderly manner so that information is not lost or difficult to locate?
This webinar will discuss proven and practical strategies to optimize the storage and organization of legacy information, paper as well as electronic. The speaker will highlight effective methods to index and organize records and integrate them so that it is easy to retrieve information. A transition from paper to electronic records will involve a myriad of challenging and complex decisions that are to be made. Attending this webinar will equip you with the necessary information and know-how to ensure that you make the right decisions.
Areas Covered in the Webinar:
- Records policy and procedures
- Records data map
- Incorporating paper records into a eCTD
- Converting paper documents into a useful electronic format
- Scanning costs and resources
- Indexing and organizing scanned records and integrating them
- Long term record storage and retrieval
- Big data - implications to the drug business
Who Will Benefit:
This webinar will benefit the following personnel from pharmaceutical and clinical trial companies:- Research & Development
- Scientists
- Regulatory Affairs
- Clinical Research (project managers, investigators, study coordinators, operations, QA and document managers)
- Legal
- Information Technology
- Validation
- Documentation
Course Provider
Charlie Sodano,
