Automate Conversion of Product and BATCH files to iVEDA approved format.

18 February, 2021 7:00 PM in Indian Standard Time

Companies are entrusted upon the responsibility to move their data from the existing DAVA portal to iVeda by 31st March 2021. With business being severely hit by the pandemic, things are not going at a pace originally planned.
In this webinar, members of the development team will describe how i2e Consulting is addressing the common concerns of converting existing Product and BATCH files in DAVA portal to iVeda approved format (XML Schema Files), along with bulk upload operations. The team will demonstrate how the system designed specifically for this purpose can accelerate your migration process with automated data extraction and processing.
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Accelerate life science innovation with consistent project and resource management practices

November 27, 2020 7:30 PM in Indian Standard Time

This webinar has been designed to focus and provide solutions for common project challenges faced by the life science industry.
The speaker will share his Project Management expertise to facilitate your strategic decision. We will then transition to the demo of Planisware Orchestra, which will showcase the management of an entire life cycle of the project on the platform. When projects last for decades, you need practices which are consistent and sustainable.
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Effective Data Integrity Program - A structured approach

October 14, 2020 8:30 PM in Indian Standard Time

The webinar is designed for establishing a Data Integrity (DI) program. With a holistic view of a company’s operation, the webinar will highlight DI’s 5-p model that global companies are effectively using to minimize exposure to data integrity audit failures. After a compendium of DI fundamentals, the webinar will quickly transition to business process considerations and interactions between people, process and equipment coupled with company culture, propensity for humans to make mistakes along with reasons etc.
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September 10, 2020 11:00 AM in Eastern Standard Time

This webinar discusses Managing the (CSV) Computerized System Validation workload.
The increased deployment of automated systems in the pharmaceutical industry means the Computerized Systems Validation (CSV) effort is also increasing. As resources are always limited, it is important to manage them efficiently and effectively.
It is easy to get lost in the data, the information, the risk assessments. Therefore, a proven, sensible, and logical approach that also satisfies the regulators is required. Read More

July 29, 2020 11:00 AM in Eastern Standard Time

Regulated organization increasing trend of dependency on a computerized system for GxP business operations are directly dependent upon underlying IT infrastructure. This certitude brings validation and quality operations related to IT infrastructure maintenance at the center of attention. In a regulated environment validated status of the GxP application is always depends on the assurance of underlying IT infrastructure. The consequence of IT infra quality operations failure can be significant. Based on the severity of risk entire region or site business operations can be at the halt or cease. Read More

July 8, 2020 11:00 AM in Eastern Standard Time

In the current ongoing pandemic situation; remote operations have become a necessity for business continuity. Document approval is obligatory to grant any authorization for many of pharmaceutical GxP business operations. Read More

June 11, 2020 7:00 PM in Indian Standard Time (India)

Effective operations strategy during a pandemic, based on the severity of outbreak would enable organizations to maintain uninterrupted manufacturing and supply of drugs, including lifesaving drugs to the end-users viz. patients, effectively. Read More

May 14, 2020 11:00 AM in Eastern Time (US and Canada)

Enabling Effective Quality and Compliance Operations Through Complexity-Considered, Risk-Based Planning

This webinar discusses how strategic approaches to Quality can provide critical enterprise contributions to your company’s operational, and financial performance. Read More