Naturotac is a DCGI(CDSCO) approved new age CRO with all necessary infrastructure to cater to the Pharmaceutical and Biotech industry, established by a group of enthusiastic professionals with a vision to set-up a premium Clinical Research Organization known for its Quality, Knowledge and Expertise. Naturotac understands the importance of quality clinical research services and our significantly experienced team strives to provide the same to our sponsors at significant cost advantages. Representing a vertically integrated CRO, we offer customised solutions to suit sponsor requirements for the full spectrum of clinical research.
The facility is located in the center of the city within a km from the railway station & the central bus stand. The facility is divided into well laid out areas defined by operations such as Clinical Research, Bioanalytical Research, Project Management & Biopharmaceutics and Quality Assurance. With doctors and paramedical staff available 24/7 the clinic consists of 160 beds with a state-of-the-art bioanalytical laboratory equipped with LC-MS/MS for analysis.
Whatever the size of your biopharmaceutical company, our global presence can help accelerate your drug development around the world. Our diverse professionals represent the best and the brightest in clinical, regulatory and market access specialties. We’re passionate about supporting your objectives and committed to partnering with you to make medicines accessible to patients who need them most.
In India and USA, we have our presence since 5 years and we have recently entered Australia to reduce the cost of early phase trial. Our experts in clinical team have almost 5 years’ experience working on 200+ early phase studies, making us an exceptionally experienced local provider within the APAC region and a partner of choice for many international biotech companies.
Early Phase services provider:
Product development in Australia
The regulatory environment in APAC offers a significant strategic opportunity for international biotech companies who can take advantage of a uniquely fast and pragmatic regulatory pathway for early phase clinical trials. Uniquely, through naturoTac Drug Development Consulting team, naturoTac is able to provide gap analysis and critical assessment of client’s pre-/non-clinical data to ensure our client’s package is ready and suitable for submission.
The simplicity and efficiency of the APAC Regulatory and Ethics (IRB) processes often means our clients can defer regulatory submissions in other regions by initiating their clinical programs and commencing subject treatment within a single review cycle of 6-8 weeks from submission.
Accelerate your clinical development program with naturoTac
Services include project management through to clinical trial monitoring, management and patient recruitment. naturoTac delivers unmatched experience as the Asia-Pacific’s leading CRO with, expert teams and deep local regulatory knowledge.
naturoTac streamlined and integrated clinical trial services are delivered by teams of professionals with strong industry and therapeutic area expertise across all phases of clinical development.
The teams also have established relationships with trial sites, key opinion leaders and Principal Investigators resulting in rapid and effective trial start-up, patient recruitment and site selection to deliver on clinical timelines.
A full range of Project Management services
Whatever the size of your biopharmaceutical company, our global presence can help accelerate your drug development around the world. Our diverse professionals represent the best and the brightest in clinical, regulatory and market access specialties. We’re passionate about supporting your objectives and committed to partnering with you to make medicines accessible to patients who need them most
Archana Malviya, PhD is founder and Chief Medical and Scientific Officer for naturoTac. In this role, she is the lead medical and scientific expert and is involved with the company’s oversight of scientific integrity, governance of Clinical Phases I – IV, Development, BA/BE studies, Clinical Data Management and Pharmacovigilance.
Archana has nearly 25 years of medical and research experience, and since 2002 she has worked in the life sciences and biotech industry. Prior to joining naturoTac as a co-founder, Archana worked in roles of increasing responsibility at IQVIA and Takeda in clinical development, pharmacovigilance, and medical affairs. She was employed as Clinical Pharmacologist as one of the faculty of Johns Hopkins School of Medicine, where she performed novel research on Oncology and Cardiometabolic disease where she holds several patents based on her research and insights.
Archana holds PhD degree from Johns Hopkins School of Medicine, USA and M.D & MBBS from AIIMS, India. She has completed specialty training in cardiometabolic disease at Johns Hopkins and sub-specialty training in cancer medicine from Johns Hopkins and the National Heart, Lung, and Blood Institute.
Naturotac is committed to offer total service satisfaction to our customers and strives to achieve the goal of excellence, through a continuous improvement of our processes, systems and services, in delivering high quality projects meeting regulatory requirements in full compliance with GCP, GLP and ensuring adherence to approved protocols, regulatory, ethical and scientific norms.
To become the preferred research partner in drug development process for our clients with true scientific spirit and delivering high quality standards within stipulated timeframe and keeping pace with latest techniques and procedures, ensuring scientific validity of all research projects and complying with global regulations.
We strive to provide exceptional customer service through flexible scheduling, quality data, efficient services and customized solutions resulting in value to the customer and company.
We are committed to strive relentlessly and constantly to improve ourselves, our team and our services so as to become the best.
We constantly strive to redefine the standard of excellence in everything we do. The only constant in life is change and we believe that in order to stay relevant we must constantly improve with society’s changing needs.
We are committed to conduct ourselves in a manner consistent with the highest standards of integrity. We are honest, ethical and fair in all our activities. In all that we do, we believe that our reputation is more important than any other short-term rewards.
We seek to understand how we can best support each other and make choices that put team before individual performance.
Naturotac is a DCGI(CDSCO) approved new age CRO with all necessary infrastructure to cater to the Pharmaceutical and Biotech industry, established by a group of enthusiastic professionalswith a vision to set-up a premium Clinical Research Organization known for its Quality, Knowledge and Expertise.
