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FDA

EU

The impact of modern Regulatory (RIM) technology on time to market

FDA

EU

The impact of modern Regulatory (RIM) technology on time to market

FDA

EU

The impact of modern Regulatory (RIM) technology on time to market

FDA

EU

The impact of modern Regulatory (RIM) technology on time to market

Different policies and submission procedures across countries and regions create a significant barrier to meeting regulatory deadlines and can easily become an intricate puzzle if there is not a centralized Regulatory (RIM) Platform to merge and automate all regulatory processes and data.

Beyond regulatory teams, RIM Platforms lead to cross-functional efficiency gains and catalyze company-wide benefits, especially in accelerating the time-to-market for new products.

Employing a RIM Platform for regulatory management enhances efficiency, reduces the risk of rejection or noncompliance, and offers comprehensive visibility across global registration processes. Beyond regulatory teams, RIM systems catalyze company-wide benefits, especially in expediting the time-to-market for new products.

#3 ways the Essenvia RIM Platform can accelerate time-to-market for new products

Essenvia RIM Platform offers a suite of capabilities enabling MedTech companies to expedite market entry and sustain their presence:

#1. Digital Forms and Templates
Essenvia offers a comprehensive library of expert-prepared templates for different products and markets and significantly reduces the time to submission.

#2. Centralized Visibility
Our Platform acts as a digital hub for regulatory data (providing a singular source of truth) and enables teams to reuse information across global applications and registrations, streamlining processes and improving visibility (including integration with eQMS, PLM, DMS or CRM).

#3. Regulatory Intelligence
The Essenvia RIM Platform provides proactive alerts on new or updated guidance and standards that are applicable to your products, offers information on competitor products, and real-time executive dashboards to review the internal status of submissions and time to completion.


Do not hesitate to book a personalized demo of the Essenvia RIM Platform to discuss your specific use cases and support your decision on whether it makes sense to adopt modern technology to streamline your regulatory work.

Our team of regulatory experts will consult with you about your specific organization's needs and provide an honest perspective on whether an RIM solution can support you.


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