We Specialize in Pharmaceutical CMC Analytical Development, Quality Control, Stability and Regulatory Affairs
Client satisfaction is the top priority and driving force for our business
Clients are billed solely for actual, documented working hours. Our goal is to help clients minimize their operating costs.
We provide competitive hourly rates without compromising the quality of our services.
Clients are not obliged to pay bonus, benefits or PTO hours.
Clients can terminate contracts at any time without penalty or the need to provide justification. No severance package or termination fees apply.
We provide remote management of CMC development and GMP manufacturing activities at contract partners.
We offer on-site, in-plant, and wet-lab technical support at client-approved premises or contract partners' labs, with prior authorization.
To meet clients' timeline target and demand from clinical studies or regulatory agencies, we are available to work beyond standard business hours—including evenings, weekends, and holidays—whenever needed.
Increase work efficiency with one single point of contact.
Minimal bureaucratic administration—We can get started once Non-disclosure Agreement is executed.
Driven by a strong teamwork spirit and can-do attitude, we welcome all types of challenging tasks within the CMC landscape of the pharmaceutical and biopharmaceutical industries.
Operating with professionalism and integrity is not only critical to successful pharmaceutical development, but also expected by regulatory agencies, and they form the cornerstone of how we conduct our business.
We fully recognize that all projects are the proprietary assets of our clients. We strictly adhere to confidentiality by signing Non-Disclosure Agreements and never disclose any project-related information to third parties.
Customers' problems are our problems. With unwavering commitment to work ethics and professional integrity, we deliver exceptional services while creating the highest value for our clients, enabling our clients to focus on their business essentials.
We carefully plan and execute the tasks based upon the clinical phase of the projects, ensuring compliance with phase-appropriate requirements from regulatory agencies such as the FDA, EMA, and IMP.
We are a reliable and trustworthy business partner, committed to continuity and responsibility—we will never terminate our services without prior notice from the clients.
