Top 5 Ways to Ensure Commercial Launch Success [Pl...
How will you manage mounting regulatory scrutiny and competitive pressures?
As healthcare spending continues to spiral out of control, pharmaceutical and biotech companies like yours face intense government regulatory scrutiny, as well as increasing pressure on product pricing and threats from competitive intrusion.
Is your firm positioned strategically to minimize the impact of regulatory and marketplace pressures on your business performance? Do you have the proper systems in place to maximize the revenue potential of your branded products and secure the future of your developmental pipeline?
Overcome barriers to success with the industry, data, and digital experts
At Collaborative, our pharmaceutical industry experts know your business and understand the pressures that you face. Our combination of industry knowledge and information systems expertise designs and delivers the technology solutions that your company needs to grow today and maintain your competitive advantage into the future.
So whether your business is an emerging biotech or a more established pharmaceutical company, look to us for best-in-class services and solutions—from clinical development to regulatory affairs, commercial operations, and beyond.
Choose onshoring: A cost-effective, high-quality delivery alternative
Collaborative offers a cost effective onshore delivery approach that balances client needs to manage cost, risk, value and time to market. Through the best mix of onsite consultants and the highly skilled resources of our onshore Collaborative Domestic Solution Center (CDSC), you get:
- Responsive, highly experienced and local SME consultants that can help you diagnose issues and develop solutions to complex problems
- US-based project delivery and managed services teams who are available during normal business hours
- Customized, high-quality support and accelerated service delivery, at competitive prices
- Our centers provide application support, validation and testing services, regulatory submission support, data analytics for both clinical and commercial operations, and develop tools and templates to help organizations shorten their COTS implementations