At Aventon Pharma Solutions Pvt. Ltd., we uphold the highest standards of quality in every aspect of pharmaceutical research, development, and manufacturing. Our unwavering commitment to innovation, regulatory compliance, and cost-effective solutions ensures that we deliver world-class pharmaceutical formulations to meet the evolving needs of global healthcare.
Experienced Leadership : Our leadership team brings over 75 years of collective pragmatic pharmaceutical R&D product development expertise. Supported by a robust scientific team proficient in Product Selection/Development, IP Development, Clinical/Regulatory Excellence, and Project Management.
Cutting-Edge Infrastructure: We offer ecosystem for high end technology capabilities for unparallelled research
Our team boasts over 75 years of combined experience in developing complex pharmaceutical dosage forms- 35 different dosage forms.
Team has proven track record of success in developing , filing and commercializing various innovative pharmaceutical, nutraceuticals & FMCG products
Our team comprises experts in QbD, DoE, formulation development, analytical chemistry, CMC write up, Data Analytics, Technology Transfer, IND enabling, BA/BE
Matrix , Osmotic, MUPS, Pelletization, in-situ implant, Emulsions, ER suspension, transdermal patch, lyohphilization, hot-melt extrusion, solvent evaporation, organogels, creams etc
We work closely with our clients to understand their unique needs and develop a tailor-made development strategy
Our e-CDMO services encompass all stages of pharmaceutical development, from pre-formulation to commercialization
Our advanced Formulation Technology Platform is designed to develop innovative and complex pharmaceutical dosage forms.
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We offer comprehensive analytical development services to support drug formulation, stability studies, and regulatory submissions.
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Our Regulatory and Data Analysis Platform provides end-to-end support for regulatory submissions, compliance, and documentation.
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We offer comprehensive dossier preparation and product registration support, ensuring smooth regulatory approvals across multiple regions.
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Our Market Analysis and Commercial Assessment services provide in-depth insights into industry trends, competitive landscapes, and market potential.
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R&D Quality Assurance Trust our expertise to safeguard the integrity, compliance, and safety of your innovations with a touch of quality.
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Committed to excellence, we ensure rigorous quality compliance and thorough audits, safeguarding industry standards and patient safety with precision, integrity, and unwavering dedication.
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Our expertise across various dosage forms and therapeutic areas ensures cutting-edge, QbD-driven solutions tailored to meet diverse pharmaceutical needs.
Ophthalmic : Multidose and Unit Dose Preserved and Preservative Free, Solutions, Suspensions, In Situ Gel Forming and Semisolids.
Nasal : Multidose and Unit Dose Preserved and Preservative Free Solutions, Suspensions Dry Powder, In Situ Gelling and Gels
Inhalation : Pressurized Metered Dose Nasals, Nebulized and Pressurized Metered Dose Inhalers, and Dry Powder Inhalers (DPI)
Complex Injectables : Multidose and Unit Dose Pre-Filled Syringes, LyphoIlised Powders, Solutions, Suspension, Microspheres, In Situ Gelling and Gels for Depot Injections.
Oral Liquids : Multidose, Unit Dose, Palatable (Taste Making), Immediate and Extended Release, Dry Powders for Solutions/Suspensions, Liquid Solutions, Liquid Suspensions, Emulsions, Nano-Emulsions
Topicals : Semisolids, Paste, medicated patches, and Liquid Formulations
Oral Solids : Immediate and Extended-Release Tablets, Soft & Hard Gelatin Capsules with expertise in Multi-particulates, and Solubility Enhancement thru Amorphous Solid Dispersion and Lipid -Based Formulation Development, Oral films Logenges, and gummies.
Aventon offers product development service to clients through selected CROs/CMOs channels, establishing scope on Technology Transfer or Supply Agreements.
Services : Formulation development, Process Development, Analytical MD and MV, Dev. Packaging development, Sourcing, Stability, Scale up, TT, Registration batch making, Dossier for submission, Process Validation and Launching
Forge alliances with CMOs to expand their product portfolio, leveraging Aventon business network for market penetration and securing supply agreements.
Services 1st axis - expansion of capabilities, 2nd axis - expansion toward new modalities, 3rd axis – expansion towards complementing service (Clinical, BE study, Toxicology etc)
Synergistic Alliance beyond manufacturing, Provisional Patent, commercially potent concepts with pronounced market differentiation. Strategically align innovation pipeline with the production & ensuring mutual amplification of market position
Services : IP creation, Patents, Niche product patent drafting and filing
Interim dossiers & PDR to CROs and CMOs, strategically positioned for product registration across non-regulated and semi-regulated markets, establishing royalty frameworks on Supply Agreements
Services : Technical document, dossier compilation, regulatory query handling, BE failure, reverse engineering etc.
