Cliantha, a full-service clinical research organization with over 75 years combined experience
10 February 2025
Cliantha Research, a globally recognized full-service Clinical Research Organization (CRO), caters to comprehensive and integrated offerings in clinical research segments like Early Phase (BA-BE & Phase I), Late Phase (II-IV), Respiratory, Tobacco Research, Dermatology, Consumer Clinical Research, Research Lab, Biometrics, Medical Services, Environmental Exposure Chambers (EECs).
Headquartered in Ahmedabad, Cliantha Research has expanded its domestic presence with three regional offices and established an international footprint in the USA (Florida and Pennsylvania) and Canada (Mississauga, Winnipeg, and Toronto)
Since its inception in 2004, Cliantha has achieved many milestones, eventually contributing to growth and success.
In 2011, a key milestone was achieved when Cliantha acquired American “HillTop Inc.”, a renowned North American Dermatology and Personal Care Clinical Research Organization (CRO) established in 1947. This acquisition enabled Cliantha to diversify into the personal care segment on a global scale, marking a significant expansion in its offerings.
In 2013, Cliantha expanded its reach within India by establishing its consumer research arm, further strengthening its market presence under the Cliantha umbrella. The technology transfer and imbibing our partner’s expertise made us stronger and more confident over the years. With over seven decades of specialized global expertise in Consumer Clinical Research, Cliantha has earned a strong international reputation by ensuring regulatory compliance and delivering a competitive advantage through its dedication to excellence.
In India, Cliantha operates in an 11,000 sq. ft. IS/ISO 9001:2015 certified facility, offering customized end-to-end services. that focus on product safety, efficacy, claim substantiation, and consumer insights for a wide range of industries including Cosmetics, Personal Care, Nutraceuticals, Herbal Supplements, and Wellness Products.
With over 5,000 studies conducted, our consumer clinical studies adhere strictly to ICH-GCP guidelines which ensures the highest quality and standards while delivering services. Our comprehensive support spans the entire research process, from protocol creation to clinical study reports, manuscripts, and publications, ensuring that we deliver robust, evidence-backed insights and helping our clients meet regulatory requirements.
Emphasizing evidence-based, data-driven insights, we leverage a dedicated pool of 22,000+ volunteers and adopt a three-fold approach to studies: clinical evaluation, subjective assessment, and advanced quantification using cutting-edge scientific bio-instruments. Our state-of-the-art arsenal includes instruments such as VISIA CR, Antera 3D, Solar Simulator, and Environmental Controlled Hot/Cold Chambers.
Cliantha offers a wide range of value-added services to cosmetic and nutraceutical companies ensuring that products meet safety, efficacy and regulatory standards. Our core services help companies enhance product development, ensure consumer safety and meet regulatory requirements in the cosmetic and nutraceutical industries. Our services include:
- – Patch sensitivity/safety testing
- – In-use safety studies
- – Consumer insights studies
- – Safety /efficacy and claim substantiation studies
- – Medical writing/ Manuscript Writing
To carry out this scientifically driven organization, we are supported by a strong and dedicated team of over 50 professionals each with advanced degrees in medical, dental, Ayurveda and Clinical Research. Their diverse expertise allows us to approach this complex process with holistic and evidence-based perspective.
To learn more or any business-related inquiry, mail: info@cliantha.com
To discover their corporate sheet in the Skinobs platform and all their testing expertise: connect for free at: Click here
CONTACT
Mrs Mansi Tandon
Email: mtandon@cliantha.com
Discover their testing services during the Exclusive webinar and
the latest evaluation trends and innovations in preclinical trials and clinical studies.
👉 Click here to register to the webinar!
– Date: Thursday 27 February 2025
– Time: 11:00am [CET] or 3:30pm [Mumbai]
– Duration: 1 hour
⭐Our speakers for this webinar
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