Home

At Aatrix we don’t do different things. We will do things differently.

Aatrix believes that people are the key for success. We are of young and dynamic professionals at work. The team is motivated by the fact that everyone on board is a vital part of the Aatrix.

Every member is free to innovate and think hence bring their strengths to contribute to the common goal of the company. Team spirit is above in the hierarchy as we believe together we can do more and better than any individual.

Industry professionals – young, dynamic and enthusiastic entrepreneurs form the core of Aatrix team. With years of relevant experience and proven track record of building and managing high performance teams.

E take pride in provide following services to our partners like Appointment Scheduling, Demographic Entry, Eligibility & Benefits Verification, Medical Transcription, Medical Coding, Charge Posting, Claims Submission, EDI Rejections, AR Follow Up, Denials Management, Patient/Provider Correspondence and Appeals Management.

Why Aatrix

Develop Innovative Solutions

We thoroughly discuss the requirement of our partner. We work hard to achieve innovative solutions that enhance physicians financial and clinical quality outcomes, while freeing up their time to focus on patient care.

Deliver Impactful Insights:

We deliver our work with best quality at affordable cost. We believe our growths in partner’s growth. We do all possible things that could help our partner to operate in most effective and efficient way.

On-Time Milestone Deliveries

We adhere and stick to high ethical standards and professional integrity in meeting and delivering TAT, SLAs and other commitments and believes in maintaining confidentiality.

Domain Experts

We are expert in our domains and believe that people are the pillars of organization.

Aatrix Solution Benefits:

  • Increase your on-going practice revenues by 15% to 25% (depending upon current patient load)
  • Reduce rejected and denied claims
  • Recover lost revenue resulting from insufficient filing
  • Higher efficiency rate approval on fist submission
  • You will have more time to devote to your patients

Why Outsourcing Work:

  • Eliminate lengthy periods of your day dealing with insurance companies.
  • No claim submission deadlines to meet
  • You don’t have to worry about the patient’s policy changes and tracking authorizations.
  • No denied or rejected claim piling up

Gains

Achieve comprehensive gains across your revenue operations.

Aatrix Biosciences is a Bio pharmaceutical Service provider and full service CRO, providing services to pharmaceutical, biotechnology and medical devices companies. We apply our innovative technologies, therapeutic expertise and a commitment to quality to help clients and partners accelerate the delivery of safe and effective therapeutics and maximize the returns on their R & D investments.

Vision, Mission and Values

Vision

Revolutionize Healthcare Sector by doing things differently and establish a new model for business. We work to be trusted by patients, a valued partner in the community, and creators of positive change.

Mission

Share One Mission – Customer’s Success

We are inspired and energized by uniting and sharing one mission. We commit ourselves and our success to our customer’s ability to achieve their business objectives, to support their mission and to better care for their patient’s.

Values

High Integrity & Transparency

Unleash the Power of Our People

Have Fun While Being the Best

Adaptable to Change

Give Respect Take Respect

About

About Aatrix

Because we strictly and strongly adhere to 7 quality management principles

• Customer focus
• Leadership
• Engagement of people
• Process approach
• Improvement
• Evidence-based decision-making
• Relationship management

Above All:

Continuous Training Sessions through sharing process Knowledge at all levels  by Experts in the Industry.

OUR VISION

Revolutionize Healthcare Sector by doing things differently and establish a new model for business. We work to be trusted by patients, a valued partner in the community, and creators of positive change.

To become a trusted business partner to our clients and their customers in achieving their business strategies with wisdom of confidence and comfort to operate with utmost efficiency.

OUR MISSION

Share One Mission – Customer’s Success

We are inspired and energized by uniting and sharing one mission. We commit ourselves and our success to our customer’s ability to achieve their business objectives, to support their mission and to better care for their patient’s.

Our Mission is to partner with our clients and their customers to empower them to make smarter decisions through our exceptionally innovative techniques of services and consulting, professional training and assistance, and information technologies that help them to succeed; Provide our employees with extraordinary challenges, fulfillment, and the opportunity to significantly enrich their careers; We are committed to provide the widest range of choices, deliver good quality and value backed up by our expertise.

OUR OBJECTIVES

To apply our innovative technologies, therapeutic expertise and a commitment to quality to help clients and partners accelerate the delivery of safe and effective therapeutics and maximize the returns on their R&D investments.

OUR VALUES

High Integrity & Transparency

Unleash the Power of Our People

Have Fun While Being the Best

Adaptable to Change

Give Respect Take Respect

Services

CLINICAL OPERATIONS

We can perform all stages of clinical trials – from feasibility to final study report – to the highest quality standards.

We have wide therapeutic experience, excellent cooperation with site staff and in-depth knowledge of local requirements. Our core expertise and focus is in the South and South East Asia, however we are able to cover the whole of Asia and many other countries through our partner CROs. Our resourcing model provides both the flexibility and local knowledge of each country that the study requires.

Monitor plays a significant role to ensure the project success.  As a company commitment to Clinical Research Excellence, we designed the role of our monitors to go beyond, than simply meeting the technical accuracy demanded by the research.

Our CRAs are trained to predict site management issues and proactively develop and implement solutions. CRAs undergo a thorough instructional regimen and are trained. This approach is employed from the earliest stages and throughout the conduct of the clinical study, to ensure the proper flow and responsiveness of the process.

All our monitors are full-time bilingual employees, equipped with laptops and are always available through mobile phones and internet when they are off site.

Whether helping your organization handle an overload of work on a single project or designing a full-service clinical program for your product, Aatrix Biosciences clinical trials management team has experience and knowledgeable staff members ready to assist you.

  • Clinical services custom-tailored to fit your needs.
  • Study document development.
  • CRA management and quality control.
  • Clinical monitoring and site management.
  • Clinical Trial Management System.
  • Investigator meeting planning.
  • Audits and preparation for audits.
  • Training.
  • Patient recruitment and retention strategies.
  • Feasibility studies.
  • Quality training of clinical associates.

 

DATA MANAGEMENT

An effective data management is the principle core for any successful clinical trials. At Aatrix Biosciences, the handling and maintaining of clinical trial data is a major part of our service offering. Our team members have sound knowledge in Medicine background, Biological sciences and also have a good experience in multiple therapeutic areas.
Our team is experienced and exposed in handling both paper and eCRF based studies. More over the team is flexible in adopting to the Sponsor specific tools to manage their data.
The robust SOP’s enable us to be on par with any of the leading players in the industry in terms of Quality deliverables.

BIO-STATISTICS :

We understand the importance of Statistical Analysis in clinical research and therefore we strive to provide quality services and solutions.
To ensure quality, we employ robust SOPs to practices. All our statistical services are based on ICH – GCP guidelines. Our team of knowledgeable and well experienced Biostatistician and Statistical Programmers are dedicated to deliver quality services across a wide range of therapeutic areas and to all phases of clinical trials by emphasizing on process optimization and accelerate timelines while ensuring quality and research cost reduction.

Some of the key areas of support include:

• Power / Sample size estimation
• Protocol preparation
• Mock tables and listings
• Edit check programming for Data Management team
• Analysis dataset generation
• Tables, Listings and Graph generation
• Statistical Analysis
• Interim and Final Report generation
• Validation programming and QC of Reports
• Integrated Summary of Safety and Efficacy
• Statistical Reports

SITE MANAGEMENT

Aatrix Biosciences performs site management services to act as the liaison between the site, the sponsor and the conduct of the study. We do this by continuous communication with every study site, starting with the collection of regulatory documents and continuing throughout enrollment, follow-up and project completion.

Aatrix Biosciences understands that site training is key to ensure proper study conduct, quality data collection and to keep our sponsors’ projects on top of the to-do list.

Our Project Managers and CRAs institute training programs for all site staff to ensuring compliance with FDA, local regulatory and ICH-GCP guidelines and adherence to the protocol as well as timely patient recruitment. We develop effective study protocol tools, newsletters and subject enrollment aids to reinforce site staff training.

Our proven comprehensive site support model involves placing a full-time, highly qualified clinical research coordinator at each study site to assist the investigators and site staff with all day-to-day study conduct activities. In addition, weekly teleconferences are scheduled with the site throughout the project that allows our staff to review study status, CRF and query completion and assist with protocol questions and any other study related activities to ensure the study proceeds in a timely manner. Aatrix Biosciences ensures all study information is current, prioritized, and available to Sponsors for effective site management.

MEDICAL WRITING

Our medical writing services are based on our extensive experience in the pharmaceutical industry and our commitment to quality, which ensures clear, concise and well-structured documents.

Aatrix Biosciences has a team of experienced medical writers with medical and scientific expertise to provide high quality clinical study documents compliant with ICH-GCP guidelines and regulatory requirements.

From protocol writing to the final study report preparation, our medical writers collaborate with bio-statisticians and project team members to produce comprehensive, submission-ready documents for all stages of clinical development.

All documents are peer reviewed to ensure medical and scientific accuracy and are subjected to continuous quality control to guarantee compliance ensuring high quality deliverable, on-time. We provide medical writing services as part of the comprehensive clinical trial program or as a stand-alone service.

Our medical writers help you in the preparation of the following:

  • Investigator brochure
  • Clinical study protocols
  • Informed consent forms
  • Study assessment questionnaires
  • Patient dairies
  • Clinical study reports – Phase I to IV
  • Abstracts and manuscripts
  • Clinical overview and Clinical Summary
  • DSMB manuals

Contact

Address:

# 1-1-230/2/8, Chikkadpally, HYDERABAD, TG 500020 IN

Email ID:

drmadhusudan@hotmail.com