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Lab For Pharmaceutical Research Facility

Drug Discovery

Piramal's Discovery Services (PDS) site in Ahmedabad, India, provide comprehensive drug discovery services, including synthetic chemistry, in vitro biology, in vitro ADME, in vivo pharmacology, DMPK, safety and toxicology services, route scouting, and non-GMP scale-up. We serve a diverse range of customers: large and mid-sized pharma companies, biotechs and start-ups, academic institutions as well as applied markets (cosmetics, food and beverage, seed, animal care) worldwide. Since commencing operations in early 2003, we have focused on delivering customer projects, growing into a team of over 300 scientists working in world-class chemistry and biology laboratories. PDS can provide forward integration with the company's drug substance and formulation sites in North America, UK & India, ensuring seamless support throughout the drug development lifecycle.

Featured Services

integrated-drug-discovery

Piramal Discovery Services (PDS) site in Ahmedabad offers integrated, high-quality services supported by a dedicated project management team. Our integrated drug discovery approach combines chemistry, biology, ADME, route scouting, and scale-up capabilities under the same roof, enabling seamless progression from hit identification to lead candidate selection. In addition, with our partner offering DMPK and early-toxicology services (GLP or non-GLP), we provide a full-package solution, coordinated by experienced project managers, ensuring efficient workflows, robust data generation, and on-time decision-making to select the best preclinical candidates. Once the preclinical candidate selected and even before, we can connect you with our Piramal network of CDMO to anticipate the next steps and increase your chances of success from the drug development up to the commercialization of your product.

Synthetic Chemistry Laboratory Services

Synthetic Chemistry Services for Drug Discovery

The specialized team at Piramal Discovery Solutions (PDS) boasts broad experience in preparing high quality small molecule NCEs which makes usone of the most rusted synthetic chemistry services providers for mg to kg scale discovery chemistry. We are proficient in developing methodologies, including the synthesis of single-step, multi-step and small arrays, as well as designing focused libraries to support our customers across all stages of the research pipeline, from hit identification to lead nomination, with a focus on timelines and confidentiality at each step.

 Access to scientific literature and databases such as SciFinder and Reaxys enables the team to modify and develop novel synthetic routes. Compound delivery is accompanied with analytical data including high-field NMR, and mass and purity by LC-MS/HPLC/GC. Also, Supercritical Fluid Chromatography aids chiral separation and generates a higher throughput. Our teams collaborate closely with biology and DMPK to optimize potency, selectivity, and developability. Synthetic strategies are selected with attention to project goals and intellectual property requirements, enabling the progression of promising compounds toward preclinical development.

Featured Services

  • Synthesis of discrete compounds and focused libraries accross a range of structural classes and complexities
  • Synthesis of building blocks, common intermediates, reference standards and impurities
  • Capabilities from milligram scale up to kilograms
  • catalyst screening
  • Route finding and Route scouting activities
  • Flow chemistry
  • Photochemistry
  • Electrochemistry
  • Live access to our 27,000+ chemical inventory database (including 16000 unique building blocks) via a secure cloud software - ChemInventory allowing faster access to starting materials
  • Efficient compound management with shipment around the world
  • IT infrastructure to assure confidentiality and easy access to data
  • Formulation 

Specialized Chemistry Capabilities

  • Chiral
  • Aliphatic, aromatic and heterocyclic
  • Carbohydrate
  • Steroid
  • Nucleoside
  • Natural product
  • Macrolides/MacrocyclesChiral
  • Linker-payload
  • Targeted protein degraders
  • Drug metabolites

In Vitro Biology Laboratory

Piramal's in vitro biology services are designed to provide best-in-class support for preclinical drug discovery to gain insights into compound activity, mechanism of action and safety. Our offerings span the research pipeline from hit identification, hit-to-lead and lead optimization, incorporating single plex or multiplex assay development, biochemical and cell-based assays. Each assay is tailored to address customer's needs and validated rigorously using tool compounds with QC established (signal: noise ratio, Z'-prime uniformity and reproducibility).

Featured Services

  • Capabilities include biochemical, cell-based assays, phenotypic models and high content imaging
  • Target engagement assays for several target classes : enzymes, GPCRs, ion channels, nuclear receptors, epigenetic  targets, Transporters, Transcription Factors
  • Dedicated intrsumentation to provide evaluation across multiple formats such as HTRF/TR-FRET, AlphaLISA, Fluorescence intensity and polarization, Luminescence and chemiluminescence, Absorbance, ELISA - single/multiplex, Ca2+/Na+/K+ flux, Flow cytometry, Quantitative and High Throughput Imaging, Mass spectrometry , Phenotypic analysis
  • Miniaturization of assays achieved by using 96 and 384 well plates
  • Stringent QC with tool compounds to generate trustworthy data
  • Different modalities: Small molecules, protein degraders, mAbs, ADCs

DMPK Services Laboratory

Reliable in vitro ADME Services for Drug Discovery

Our in vitro facilities deliver comprehensive services including absorption, distribution, metabolism, and excretion (ADME) solutions. These services support faster and more informed decision-making in drug discovery programs or as standalone offerings and help to reduce the risk of costly late-stage failures.

Clients benefit from cost-efficient, standardized, and customized assays for assessing key ADME parameters, ensuring precise and reliable results tailored to their unique project requirements.

Featured Services

  • Physicochemical screening
    • Aqueous solubility (Thermodynamic and Kinetic method, in biorelevant media)
    • Log P (Octanol/water)
    • Log D (Octanol/PBS)
    • pKa measurement available at Sellersville site
    • Chemical stability
    • Blood to plasma partitioning
  • Permeability and transporters
    • PAMPA
    • Cellular permeability (Caco2, MDCK wild type, MDCKII - MDR1, MDCKII-BCRP)
    • p-gP and BCRP substrate identification
  • Protein binding
    • Plasma protein binding
    • Microsomal binding
    • Hepatocytes binding
    • Tissue binding
  • Drug Metabolism
    • Hepatocyte Stability
    • Microsomal Stability
    • Plasma Stability
    • Blood stability
    • Fecal stability
    • Glucuronidation stability
  • Drug Drug interactions
    • CYP inhibition assays (endpoint or time dependant)
    • CYP phenotyping
    • UGT1A1 inhibtion
  • Metabolite Identification (without structure elucidation) : Hot spot analysis
    • Glutathione trapping
    • Reactive metabolite assessment
  • Safety
    • Herg binding (FP)
    • Ames and micronucleus (through a third party)
    • Cell cytotoxicity 

Bioanalytical Services for Small Molecules (non-GLP)

  • Method development
  • Method Validation
  • Bio-sample analysis

In-Vivo-Biology

For more than 10 years, we have partnered with trusted service providers for in vivo pharmacology, DMPK and toxicology services for a full characterization of your compound. The facilities ensure the highest standards of animal welfare and holds AAALAC accreditation, and are also GLP-accredited. Our partners offer validated diseases models across multiple therapeutic areas, as well as a comprehensive portfolio of DMPK assays for a complete characterization of your compound. Lastly we also offer non-GLP and GLP toxicology studies to evaluate systemic and local toxicity following single or repeated doses.

In Vivo Pharmacology

  • Oncology
  • metabolic diseases
  • Pain, inflammation
  • Neurology
  • Dermatology
  • Woman Health
  • Organ health
  • others

DMPK

  • Rat and mouse
  • Single or cassette dosing
  • Route of administration PO, IV,IP,IM, SC, IT
  • Tissue distribution
  • Excretion studies
  • Bioavailability studies

Toxicology (GLP/ non GLP)

  • Dose range finding
  • Maximum tolerated dose
  • Mammalian toxicology
  • Genetic toxicology
  • Immunotoxicity
  • Neurotoxicity
  • Bioanalytical

Reliable DMPK Services for Drug

Reliable in vitro ADME Services for Drug Discovery

Our in vitro facilities deliver comprehensive services including absorption, distribution, metabolism, and excretion (ADME) solutions. These services support faster and more informed decision-making in drug discovery programs or as standalone offerings and help to reduce the risk of costly late-stage failures. Clients benefit from cost-efficient, standardized, and customized assays for assessing key ADME parameters, ensuring precise and reliable results tailored to their unique project requirements. In addition, for more than 10 years, we have partnered with trusted service providers for in vivo pharmacology, DMPK and toxicology services for a full characterization of your compound. The facilities ensure the highest standards of animal welfare and holds AAALAC accreditation, and are also GLP-accredited. Our partners offer validated diseases models across multiple therapeutic areas, as well as a comprehensive portfolio of DMPK assays for a complete characterization of your compound. Lastly we also offer non-GLP and GLP toxicology studies to evaluate systemic and local toxicity following single or repeated doses

ADME services

  • Physicochemical screening
    •  Aqueous solubility (Thermodynamic and Kinetic method, in biorelevant media)
    • Log P (Octanol/water)
    • Log D (Octanol/PBS)
    • pKa measurement available at Sellersville site
    • chemical stability
    • blood to plasma partitioning
  • Permeability and transporters
    • PAMPA
    • Cellular permeability (Caco2, MDCK wild type, MDCKII - MDR1, MDCKII-BCRP
    •  p-gP and BCRP substrate identification)
  • Protein Binding
    • plasma protein binding
    • microsomal binding
    • hepatocytes binding
    • tissue binding
  • Drug Metabolism
    • Hepatocyte Stability
    • Microsomal Stability
    • Plasma Stability
    • blood stability
    • fecal stability
    • glucuronidation stability
  • Drug-Drug interaction
    • CYP inhibition assays (endpoint or time dependant)
    • CYP phenotyping
    • UGT1A1 inhibtion
  • Metabolite Identification (without structure elucidation)
    • Hot spot analysis
    • glutathione trapping 
    • reactive metabolite assessment
  • Safety 
    • Herg binding (FP)
    • ames and micronucleus (through a third party)
    • cell cytotoxicity  

In vivo services

  • DMPK: 
    • rat, mouse
    • single and cassette dosing
    • administration routes PO, IN, IP, IM, SC, IT
    • tissue distribution
    • excretion studies
    • bioavailability studies
  • Early toxicology:
    • GLP and non-GLP
    • Dose range finding (DRF)
    • Maximum tolerated dose (MTD)
    • toxicology (mammalian, genetic, immunotoxicity, neurotoxicity)
  • Efficacy studies in a broad range of validated models covering several therapeutic areas: oncology, pain, inflammation, neurology, metabolic, woman health...

Bioanalytical services for small molecules

  • Method development
  • Method Validation
  • Bio-sample analysis
Non-GMP Kilo Lab Service

Our fully equipped kilo lab enables the rapid development of scalable and robust chemical processes using advanced methodologies with speed and quality. This capability is critical for ensuring quick supply during the early development phase and for evaluating the scalability of the original process. Our team can also work closely with the development expert for a seamless transition to GMP production batches

Piramal Discovery Solutions, Ahmedabad

Our Ahmedabad facility is a Centre of Excellence for formulation development and clinical batch manufacturing of oral solid dosage forms. It has been accredited by regulatory organizations like MPA Sweden, Fimea Finland, and USFDA, among others, and is also ISO-14001 and 45001 compliant.

Piramal Pharmaceutical Development Services, Ahmedabad

Centre of Excellence for Formulation Development
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A Glimpse into Our Next Chapter: Drug Discovery

Piramal Pharma has over 60 years of expertise in small molecule API development and manufacturing. Our global facilities are equipped to meet your drug substance needs, with dedicated development resources worldwide. As a reliable supply chain partner globally, we support your drug substance development goals.

API Development
API Clinical & Commercial Manufacturing
Generic APIs
Special API Capabilities
  • API Development

    API Development

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    Development

    We offer comprehensive support for custom API development, covering Route Scouting, Pre-GMP Kilo Lab, Process Development, and Analytical Development, with expertise and flexibility.

  • API Clinical & Commercial Manufacturing

    API Clinical & Commercial Manufacturing

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    Development

    We offer manufacturing services at lab, kilo, and pilot scales, catering to preclinical studies, all stages of clinical trials, and commercialization, providing quantities ranging from milligrams to kilograms.

  • Generic APIs

    Generic APIs

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    Development

    Piramal’s Generic API division provides a diverse range of off-patent APIs tailored for global markets.

  • Special API Capabilities

    Special API Capabilities

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    Development

    Piramal’s Riverview facility offers High Potency API (HPAPI) services. Our teams are experts in the cGMP production of highly potent compounds, from grams to kilograms. With over 50 years of experience in manufacturing, handling, and containment of highly potent compounds, we prioritize safety and quality in all our operations.

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