PRADO

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Fastest Growing

Asia's Fastest Growing Preclinical Contract Research Organisation

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What Is PRADO

PRADO, Preclinical Research and Development Organization Private Limited is one of the emerging, global, independent market leaders in providing preclinical services. Following services are provided by PRADO – Toxicity Testing (In-Vitro and In-Vivo), Development of Animal Models for Human Diseases, Pharmacokinetic Studies, Biocompatibility Studies and Pathology Services. Determination of the Permitted Daily Exposure (PDE) and Occupational Exposure Level (OEL) of chemicals in compliance with EMA guidelines. Based at Pune India, PRADO is developing an outstanding reputation for providing excellent services and superior values. Our scientific data is of highest quality and our reports have excellent acceptance record with regulatory agencies, facilitating quick product registration and approval.

PRADO supports Pharmaceutical, Biopharma, Biotech, Medical Device, Pesticides and Agrochemicals, Food,Vaccine and Animal Health Industries by providing quality and cost effective preclinical services to meet their regulatory requirements. PRADO has all required technical expertise, research and development skills to provide excellent services. At PRADO, we understand how important in the on-time delivery for meeting the goals for regulatory submissions. We aim to work closely with our clients to understand their preclinical needs and develop program to meet their goals in timely manner. Thus, PRADO can be a strategic and scientific, yet responsive, flexible and trust worthy partner for your pre-clinical support.

WHY PRADO

Mission

Vision

Values

Quality Policy

Certifications

Services We Provide

Toxicologservice

Toxicology

Discovery and GLP Toxicity Studies. Acute, Subacute, Sub-chronic and Chronic Toxicity, Inhalation Toxicity, Genotoxicity Developmental and Reproductive Toxicity.

Pathology

Clinical Pathology (Haematology, Clinical chemistry, Urine Analysis), Histopathology slide preparation and evaluation. Special Staining and Immunohistochemistry.
pharmok

Pharmacokinetic

Pharmacokinetic and Tissue Distribution studies with single, multiple and cassette Dosing. Species- Rats, Mice, Rabbits, Pigs and Dogs (3rd party collaboration).
invitro-Genotoxicity

Genotoxicity

Reverse Mutation Assay (Ames Assay, Mini Ames), Micronucleus Test (MNT), Chromosomal Aberration Assay, Cytotoxicity Tests, Hemocompatibility,…
homebio

Biology

Development of animal model of human diseases. E.g. Inflammation and Pain, Metabolic Disorders, Antipsychotic Activity, Osteoporosis, Wound Healing…
biology4x4

Biocompatibility

The interaction between a medical device and the human body need to remain effective and safe over the lifetime of both the device as well as its recipient.

Services We Provide

Toxicology

Discovery and GLP Toxicity Studies. Acute, Subacute, Sub-chronic and Chronic Toxicity, Inhalation Toxicity, Genotoxicity Developmental and Reproductive Toxicity.

Pharmacokinetic

Pharmacokinetic and Tissue Distribution studies with single, multiple and cassette Dosing. Species- Rats, Mice, Rabbits, Pigs and Dogs (3rd party collaboration).
Routes- Oral, IV, IP, SC, IM, Intra-nasal, Ocular.

Pathology

Clinical Pathology (Haematology, Clinical chemistry, Urine Analysis), Histopathology slide preparation and evaluation. Special Staining and Immunohistochemistry

Biology

Development of animal model of human diseases. E.g. Inflammation and Pain, Metabolic Disorders, Antipsychotic Activity, Osteoporosis, Wound Healing or any other model as per sponsor requirement.

Genotoxicity

Reverse Mutation Assay (Ames Assay, Mini Ames), Micronucleus Test (MNT), Chromosomal Aberration Assay, Cytotoxicity Tests, Hemocompatibility, Device Implantation, Irritation studies.

Industries We Serve

PHARMACUETICAL

The pharmaceutical industry discovers, develops and market the pharmaceutical drugs for use as medications to be administered to patients.

BIO-PHARMA

Biopharmaceuticals and Biotechnology are becoming increasingly importantas novel and less toxic therapeutics for human disease.

Medical Devices

The determination of the safety or biocompatibility of a device in a biological host environment is critical step in the development of an entire...

AGROCHEMICAL

At PRADO, we understand the need for accurate and reliable data for regulatory submissions such as those of the Central Insecticide Board.

Food

Biopharmaceuticals and Biotechnology are becoming increasingly important in the development of novel and less toxic

Vaccine

Infectious diseases cause an overwhelming number of deaths around the world and their clinical management is often hampered by the emergence...

Stem Cell

Stem cell therapy, also known as regenerative medicine, promotes the repair response of diseased, dysfunctional or injured tissue using...

Risk Assessment

Setting health-based exposure limits for use in risk identification in the manufacture of different medicinal products in shared facilities...

Facilities

PRADO’s Animal Research Facility (ARF) has been designed to meet the global standards of conducting experiments on small laboratory animals. The ARF has approvals from CPCSEA, Ministry of Environment and Forests, Government of India.Know More

The Pathology department at PRADO, have specially designed laboratory areas for histopathology and clinical pathology. A spacious necropsy room is available for blood collection, plasma separation, conduct of gross pathology examination, organ weights and organ collection. Know More

At PRADO, Quality Assurance Unit (QAU) is separate department, established in accordance with the requirements of OECD principles of GLP. QAU conducts, study based, facility based and process-based inspections, as per the standard operating procedures (SOPs).Know More

At PRADO, a designated, GLP compliant Test Item Control Office (TICO) is present. The TICO area is separated based on different types of test items such as pharmaceutical, biopharmaceutical, stem cells, medical devices and agrochemical etc.Know More

PRADO understands its Corporate- social responsibility, towards this PRADO has established solar system to save the electricity and making use of natural renewable energy. For processing of facility waste, bio-digester system has been in place. Know More

The safe and secure storage of the facility and study related data and material is required for OECD principles of GLP. PRADO has suitably designed and constructed separate Wet and Dry Archives. Availability of ample space within the archives to accommodate archived records and material. Archiving procedure are ensured through strict compliance with SOPs.Know More

The in-vitro laboratories at PRADO are spread over 600 sqft and are designed for carrying out genotoxicity and biocompatibility studies, including cytotoxicity studies.Know More

Our Team Members

Dr. Pralhad Wangikar

Director and CEO

Ms. Ila Wangikar

Managing Director

Dr. Pradeep Deshmukh

Deputy Test Facility Management