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Commercialization

Commercialization Challenges

Developing a drug, from an initial concept in a laboratory all the way to the hands of patients, is a monumental undertaking involving decades of research and testing, and billions of dollars. The potential for a catastrophic setback during the discovery, development, preclinical, clinical, and FDA review stages of a new product’s lifecycle make the commercialization stage that much more rewarding, and important.

As a new product is finally introduced to the public during the commercialization stage, much of the potential for success or failure lies in the hands of the manufacturer. Though marketing and sales personnel play a vital role in bringing a new drug to market, quality, uninterrupted production is undeniably the most important piece of a successful product launch. The reputation of the drug and the company providing it are particularly vulnerable during the introductory period. Thanks to the proliferation of media, quality control and supply failures are now public information.

Why Collaborate With EFC Pharma?

It’s no secret that properly executed commercialization is essential to the success of a new product.

Commercializing a new product presents equal parts opportunity and challenge for leading-edge pharmaceutical and biotechnology firms. As companies invest considerable sums into developing new solutions for patients, pressure to successfully bring these products to market begins to mount.

With a limited window in which to capitalize on their latest innovation, these firms can see a massive ROI from partnering with compliance and production specialists.

Reducing delays in the commercialization stage strengthens a pharmaceutical company’s position and increases brand confidence among patients and the medical community. EFC Pharma is well-versed in what is required for a successful product launch and is ready to help your firm take full advantage of opportunities in the marketplace.

Capabilities That Count

Maximizing R&D investment by streamlining and simplifying the commercialization process is done through our relationships with world-class pharmaceutical manufacturers. These facilities are industry leaders, possessing a wide range of capabilities, including but not limited to:

GMP Commercial Scale Production
Liquid filling
Lyophilization
Integrated Support Services
A variety of delivery formats

Pharmaceutical companies bringing innovative drugs to market stand to benefit greatly by meeting and exceeding regulatory requirements. By eliminating costly 6-12-month compliance-driven delays, our clients can provide an uninterrupted supply of their newest solutions. EFC Pharma and our network of manufacturers possesses a thorough understanding of all the considerations of the commercialization stage, ensuring optimal speed to market for innovative products.

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Powering Your Most Profitable Relationships.


EFC Pharma proudly serves the pharmaceutical industry as the leading development, production, site transfer, and compliance specialists. Our relationships throughout the U.S and international markets allow us to facilitate the most profitable solution for your manufacturing and development obstacles. For further information about our production and development services, please contact us here.