Why Integrated?

CRO SELECTION IS A RISKY BUSINESS -

WE MITIGATE THIS RISK FOR YOU.

When it comes to choosing a CRO, we know you've wealth of options. We understand what's at stake for you and how critical it is to find a CRO team that’s not only competent, but also has the vital know-how and expertise to guide you to a successful trial. While every CRO promises stellar quality data, flawless outcome and unbelievable customer satisfaction, very few ever come close to meeting such promised expectations. CRO selection is definitely a 'Risky business'.

At Integrated, we've one word solution to mitigate this CRO selection risk, 'Transparency'. Even before we're bestowed with the privilege of working on your project, we’ll walk you through an entire rundown of how we’re going to be approaching your applicable process – from start to finish. We believe in working together as a team and pride ourselves on proactively keeping you updated with results and upcoming course of actions.

WE'RE EASY TO WORK WITH

While it may sound like a cliché, our first priority is quality of service from a group that is 'Easy to work with'. We value your input, encourage feedback and listen proactively, so we understand your expectations and exceed them.

“We are committed to your success”

HANDS FREE CRO OVERSIGHT EXPERIENCE

We make your job easier!

Providing you a hands-free CRO oversight experience allows for delegation of projects freeing your time and resources to focus on other aspects of clinical development. You'll also efficiently manage more studies with minimal resources. We want you to know that working with you is a privilege, and your trust is something we must earn.

TECHNICAL EXPERTISE - INNOVATIVE PROCESS

Our expertise lies in taking complex tasks and devolving them into a more relative and simple form. Our processes are carefully designed to be implementable and uniform across all projects, while maintaining comprehensive industry standards. We keep our SOP's simple and unambiguous to maintain ease of reference while performing associated tasks, as well as comprehensive quality control to ensure compliance and uniformity for all project related documentation and activities.

REGULATORY GUIDELINES & ETHICS COMPLIANCE

One of the most important aspects of clinical research is generating clean, scientific databases in preparation for statistical analyses and compliance with regulatory guidelines. We achieve this by aligning our processes and practices to strictly conform to industry regulations such as GCP, GMP, GCDMP, and CDISC standards.

LIMITED FINANCIAL EXPOSURE

"The high cost of developing drugs shouldn’t be a badge of honor for drug firms; there’s no reason it has to be this expensive"

We realize your commitment to offer patients with affordable treatment and we wish to be part of your cause by offering cost-effective solutions. We feel that you don't owe to pay more to cover large CRO overheads. And we must be able to offer cost-effective solution without compromising data quality or integrity.

We leverage on highly advanced technological which automates Clinical Trial Management process, effectively reducing efforts and time required to complete any task.