Fastest Growing
Asia's Fastest Growing Preclinical Contract Research Organisation
Click For Virtual Tour
Welcome To PRADO, Preclinical Research and Development Organization Private Limited
Where We Are Dedicated To Providing Notch Services That Cater To Your Research Needs
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
What Is PRADO
PRADO, Preclinical Research and Development Organization Private Limited is one of the emerging, global, independent market leaders in providing preclinical services. The 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 in Pune India, PRADO is developing an outstanding reputation for providing excellent services and superior values. Our scientific data is of the highest quality and our reports have excellent acceptance records with regulatory agencies, facilitating quick product registration and approval.
PRADO supports Pharmaceutical, Biopharma, Biotech, Medical Devices, 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 programs to meet their goals in a timely manner. Thus, PRADO can be a strategic and scientific, yet responsive, flexible, and trustworthy partner for your pre-clinical support.
Why PRADO
Certifications
Services We Provide
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.
Pharmacokinetic
Pharmacokinetic and Tissue Distribution studies with single, multiple and cassette Dosing. Species- Rats, Mice, Rabbits, Pigs and Dogs (3rd party collaboration).
Genotoxicity
Reverse Mutation Assay (Ames Assay, Mini Ames), Micronucleus Test (MNT), Chromosomal Aberration Assay, Cytotoxicity Tests, Hemocompatibility,…
Biology
Development of animal model of human diseases. E.g. Inflammation and Pain, Metabolic Disorders, Antipsychotic Activity, Osteoporosis, Wound Healing…
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.
Service we provide
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.
Pharmacokinetic
Pharmacokinetic and Tissue Distribution studies with single, multiple and cassette Dosing. Species- Rats, Mice, Rabbits, Pigs and Dogs (3rd party collaboration).
Genotoxicity
Reverse Mutation Assay (Ames Assay, Mini Ames), Micronucleus Test (MNT), Chromosomal Aberration Assay, Cytotoxicity Tests, Hemocompatibility,...
Biology
Development of animal model of human diseases. E.g. Inflammation and Pain, Metabolic Disorders, Antipsychotic Activity, Osteoporosis, Wound Healing...
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
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...
-
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...
-
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.
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
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
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, 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
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
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 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
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
Facilities
Animal Research Facility (ARF)
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
Pathology
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.
Quality Assurance Unit
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).
Test Item Control Office
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.
Environment, Health and Safety
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.
Archives
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.
In Vitro Facility
The in-vitro laboratories at PRADO are spread over 600 sqft and are designed for carrying out genotoxicity and biocompatibility studies, including cytotoxicity studies.
Certification & Awards
- PRADO received recognition by DSIR (Department Of Scientific & Industrial Research,Govt. Of India).
- PRADO has successfully received GLP certificate at our new location. Certificate No:GLP/C-168/2021
- We have successfully completed the relocation inspection of our Test Facility by NGCMA.
- PRADO received GLP certification at previous location - Certificate No: GLP/C-127/2018. We have relocated our test facility, awaiting renewal of GLP certificate.
- PRADO Received 'Fastest Growing Indian Company Excellence Award 2017' by International Achievers Conference at Bangkok, Thailand.
- Our CEO and Director received 'Indian Leadership Award for Industrial Development' from All India Achievers Foundation in 2017.
- Received CPCSEA certificate (1723/PO/RcBiBt/13/CPCSEA). Our new facility has also been inspected and approved by CPCSEA.
Certification & Awards
- PRADO received recognition by DSIR (Department Of Scientific & Industrial Research,Govt. Of India).
- PRADO has successfully received GLP certificate at our new location. Certificate No:GLP/C-168/2021
- We have successfully completed the relocation inspection of our Test Facility by NGCMA.
- PRADO received GLP certification at previous location - Certificate No: GLP/C-127/2018. We have relocated our test facility, awaiting renewal of GLP certificate.
- PRADO Received 'Fastest Growing Indian Company Excellence Award 2017' by International Achievers Conference at Bangkok, Thailand.
- Our CEO and Director received 'Indian Leadership Award for Industrial Development' from All India Achievers Foundation in 2017.
- Received CPCSEA certificate (1723/PO/RcBiBt/13/CPCSEA). Our new facility has also been inspected and approved by CPCSEA.
Our Team Members
Dr. Pralhad Wangikar
Director and CEO
Ms. Ila Wangikar
Managing Director
Dr. Pradeep Deshmukh
Deputy Test Facility Management
Our Team Members
Dr. Pralhad Wangikar
Director and CEO
Ms. Ila Wangikar
Managing Director
Dr. Pradeep Deshmukh
Deputy Test Facility Management