As life science companies move forward and innovate from pharmaceuticals to medical devices and more, companies need to keep in mind that their day-to-day tech needs to move with them. Digital transformation has become a strategic necessity.
Here, we take you - our valued customer – through what digital transformation is looking like for document collaboration in the life science industry.
Contact your account managerFind out how we can support you further with our solutions.
Transform the way you work
To be able to grow efficiently, productively and let’s be honest, at a faster pace than the competition, you need a solution that can offer you a slick, fully integrated and regulation compliant solution to collaborate both internally and externally.
Ideagen PleaseReview can offer you a full suite of features that can reduce your document review cycles by up to 65%. You can also cut review meetings down by 60%, saving ample time to work on other projects that require your attention.
Digitally transform the quality of your documentation whilst protecting your IP. No matter where you are or your document type, you can leverage Ideagen PleaseReview and be confident in your actions.
Find out how PleaseReview has revolutionized document collaboration for the life science industry by downloading our success stories.
Access in seconds
Implementing a secure, cloud-based solution you can have access to within seconds.
Fully complying with regulatory and compliance measures set out for the life science industry, upholding best-practices.
Being audit ready with a complete audit trail and reconciliation reports.
Streamline total process
Streamline the creation, co-authoring, and review of all documentation, from labelling to intensive reports.
Find out how one company reduced their process from 120 to 42 days
PleaseReview is integrated with Veeva Vault as a Silver Technology Partner
The simple and intuitive solution empowers multiple people to review, co-author and redact documents securely and simultaneously in the same platform.
Faster document authoring and review
Fewer review cycles
Shorter review meetings
Higher quality documents
Expedite drug development and working with tight deadlines
Developing a new drug or medical device can be a lengthy endeavour and cost billions of dollars. When it takes an average of 12 years to progress a drug from discovery to market, you do not want slow and outdated processes to be the reason your competitors beat you to the finish line.
With life science companies now turning to SaaS solutions to improve auditability, data management, and document collaboration, take a look at how PleaseReview can help you accelerate your time to market.
Ideagen’s PleaseReview helps Lexicon Pharmaceuticals save hundreds of hours by reducing document review timesDownload case study
UniQure uses PleaseReview to get transformational gene therapies to patients quicker.Download case study
PleaseReview Success Stories
In response to the COVID-19 crisis, the top 5 approved vaccines were developed in record time with the help of PleaseReview, our real-time document collaboration tool.Find out more