Program Management

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Navigating Regulatory CMC Success: Expert Services for Drug Development and Commercialization

Enkrisi’s Project Managers have strong knowledge of FDA regulations and are the primary point of contact for project coordination. They provide regulatory and product development guidance, accompany sponsors to FDA meetings, and participate in teleconferences.

Enkrisi’s project management services are comprehensive and practical, helping clients navigate the regulatory landscape, stay up-to-date and compliant with evolving industry practices, and achieve project success.

How we can help

An organized and efficient project manager can be the difference maker in the execution of a successful project. Enkrisi Regulatory Project Managers:

How we can help

An organized and efficient project manager can be the difference maker in the execution of a successful project. Enkrisi Regulatory Project Managers:

What makes Enkrisi your ideal choice?

Project management services provided by Enkrisi Project Managers are comprehensive and practical for the successful execution of projects. Their robust knowledge of FDA regulations and guidance, as well as their experience interacting with FDA project managers and reviewers, make them valuable resources for US Agent clients who seek to navigate the regulatory landscape. Additionally, their ability to follow trends and provide regulatory and product development guidance can help clients stay up-to-date and compliant with evolving industry practices.

As primary points of contact for project coordination, Enkrisi Project Managers can help streamline the writing, review, strategy discussions, publishing, and application life cycle maintenance activities critical to achieving project success. They can also advise on optimal practices for creating efficient and reviewer-friendly applications, which can improve the likelihood of a successful review outcome.

Finally, Enkrisi Regulatory Project Managers can provide regulatory and submission guidelines to clients and accompany sponsors to FDA meetings, which can be instrumental in obtaining regulatory approval. By participating in teleconferences, they can provide valuable insights and expertise to support clients throughout the project lifecycle. Overall, our project management services are a valuable asset to any organization seeking to bring a product to market while complying with regulatory requirements.

Your success,

stories

Enkrisi’s Regulatory Strategy Team: Highly Skilled and Effective in the Pharmaceutical Industry

As someone who has worked in the pharmaceutical industry for several years, I can say without hesitation that Enkrisi’s Regulatory strategy team is top-notch. Their team of experts is highly skilled at navigating the complex regulatory landscape, and they are always on top of the latest developments in the industry. I highly recommend their services to anyone looking to bring a new drug to market. Enkrisi’s Regulatory Consultants have a strong history of effective communication. They can author critical messages supported by scientifically-cohesive narratives, reports, and data summaries for your investigational and marketing submission documents.

Lisa D

VP, Regulatory Affairs and Quality Assurance

Enkrisi’s Quality and Expertise Critical to Drug Sponsor Success

Since transitioning to a drug sponsor role, I have continued to rely on Enkrisi for their guidance and assistance in ensuring our drug product meets regulatory standards and is ready for commercial distribution. Your team’s attention to detail and commitment to quality have been crucial to our success. Enkrisi’s experienced contract regulatory writers can provide Common Technical Document (CTD) content, FDA Briefing Books, meeting minutes, slides, and more to help you meet or beat every deadline, challenge and improve document quality, and become someone you can unquestionably rely on.

Lynn G

SVP Regulatory Affairs

Enkrisi: Top-Tier Drug Development Support for Due Diligence and Licensing Deals

Enkrisi’s drug development support services are among the best I have ever encountered for due diligence and licensing deals. Their team of experts is highly knowledgeable about all aspects of CMC operations management, and they are always willing to provide guidance and support to help their clients succeed. They are genuinely passionate about what they do and are committed to helping their clients bring new, innovative drugs to market.

Brian S

Operating Partner - Life Sciences

Enkrisi: Exceptional Drug Development Support from Research to Commercial Distribution

Enkrisi’s drug development support is truly exceptional. From the earliest stages of research to the final phases of clinical trials, their team is there every step of the way, providing guidance and support to help ensure success. Their expertise in CMC operations management is particularly impressive, and they are always willing to go above and beyond to help their clients achieve their goals. If you are developing a pharmaceutical drug product for commercial distribution, seeking expert assistance with CMC regulatory work from Enkrisi can help you manage and lower regulatory risk and avoid regulatory delay.

Jamie D

Director of CMC

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The VirtualPharm Podcast is an audio series that covers topics related to compliance and regulatory affairs in the Lifesciences industry. Each episode, hosted by an expert in the topic with decades of experience, offers listeners detailed insight into the changing regulatory environment.

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The PathFinder focuses on relevant topics such as regulatory developments, compliance trends, legal updates, enforcement actions, industry insights, and best practices. Articles are written by experts in the field to ensure accuracy and help sponsor companies stay informed about changes in their regulatory environment.

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