Enduring value for human life, Arouse Pharma Private Limited is a start-up pharmaceutical company based out of Hyderabad and promoted by highly talented pool of scientists. Innovative Research and Development is the backbone of Arouse Pharma Private Limited with customers at the core and employees at the front is our way of doing.
Expertize in
Developing and optimizing cost-effective synthetic processes for APIs and intermediates both for use in commercial and clinical studies.
Our vision is to deliver highest quality affordable life-saving medicine with an integrated approach of scope, expertise and resources.
Our mission is to become a hub in the development of pharmaceuticals with strong motive of innovation and Excellence in everything we do.
END TO END TECHNICAL SUPPORT FOR FASTER APPROVALS
For any product related enquiry please mail us : BD@arousepharma.com
Arouse Pharma has successfully demonstrated the supply of high-quality APIs and Intermediates for the following therapeutic class of drugs: Anticancer, Antivirals (HCV and HIV), Antibiotics, Antihistamines, Antidiabetic, Nonsteroidal anti-inflammatory, Antihypertensive, Anticoagulants and calcium channel blocker drugs for Regulated (USFDA, EMA, COFEPRIS, ANVISA, PMDA, etc..) and Emerging markets.
We, Arouse Pharma also offer custom synthesis services which are tailored to meet the customer requirements from early process development to till commercial supply.
Amide coupling with various activating agents
Glycosidation with pyrimidine and purine derivatives
Sulfide formation with thiol
Methylating agent: CH3I, CH3MgCl, iPrMgCl etc
Strong organometallic bases: BuLi, LiHMDS and n-HexLi,
In situ generation of Borane (BH3)
Azidation: NaN3 & DPPA
Enzymatic resolution
Diastereomeric crystallization
Synthesis using Chiral Auxiliary
Asymmetric reduction
Friedel-Craft Acylation,
Sugasawa reaction
Halogenation using NIS, NCS
Suzuki coupling, Sonogashira coupling
Wittig reaction, Julia-Kocienski Olefination
Modified Buchwald-Hartwig cross-coupling
Catalytic Hydrogenation
Various metal hydride reduction (NaBH4, LAH, LTTBA, Red-Al etc)
Various oxidation with TEMPO, DDQ, MCPBA and H2O2
Dr. Rajesh Kumar has 23+ years of rich cross functional experience in Integrated Generics product development covering route scouting, wet chemistry, scale up, quality management, patent evaluation and regulatory filings of general and oncology products. Wealth of knowledge on Analytical, IPR, quality, regulatory, ICH, ISO, cGMP, USFDA, EDQM guidelines. Developed Generics, NCEs, Oncolytics, in leading multinational Pharmaceutical Organisations including multiple global-led organizations and filed several DMFs, patents, and international journal. He is a Ph.D. in Chemistry and PG Dip in Patents law.
The Research & Development process of Drug development is a critical phase in Pharmaceutical industry. The team in Arouse Pharma Private limited is led by a talented scientist having multiple skills from product portfolio management to commercialisation,... he leads a team of scientists from R&D;, technology transfer and projects. He is an expert in handling DMF deficiencies, identification of high complex impurities, genotoxic impurities, Polymorph screening of APIs, Technical Write-Up of Scientific results and manual scripts. He has a comprehensive understanding of the market strategy, business planning, developing strategic sourcing channels at the lowest total cost and creating value for customers and stakeholders through operational excellence by optimizing and emphasizing the organization’s commercial product portfolios. The R&D; team is having effective expertise in process development with experience in producing non-infringing, cost-effective and eco-friendly process by applying principle of Quality by Design as a more systematic approach to product development.Read more
The Analytical Research and Development team is led by an industry pioneer with vast experience in working with multiple global-led companies. He is a motivated and highly persistent professional, works collaboratively with... other functional areas outside the Analytical department to advance projects. He is instrumental in developing, troubleshooting, and utilizing new analytical methodologies to support process development of starting from small molecules to complex Peptides, oligonucleotides etc. The team under his guidance performs the method development, transfer, verification, and qualification in support of process and formulation development with exceptional documentation skills. Team can support new product development with advanced method development, validation and generation of technical data in support of drug substance regulatory requirements by ensuring cGMP/GLP in day-to-day work in the labs.Read more
Process engineering team at Arouse Pharma Private limited is vested to transform Laboratory designed processes to increase productivity with safety and profitability. Having a decade of professional experience in multiple global-led companies, the Team leader is enthusiastic and... gets involved all the way from development to commercialization. The team under his supervision, has enriched experience in Equipment mapping, Safety conceptions, Scale-up, zero effluent ideology, and keep up to date on emerging technologies. Team is especially strong in being consciously cost driven, Hazop principles, handling high volume Grignard reactions, high temperatures and different novel crystallinity molecules, critical molecules like semisynthetic polysulfates, Heparins, Antivirals, Anticoagulants etc.Read more
Regulatory affairs and Development quality assurance teams are under single supervision who has more than a decade of experience in managing various aspects of Pharma Regulatory submissions & related Compliance Activities.... She is well versed in managing US & EU market regulatory filings, hands-on experience in Genotoxicity Assessment for various products, having adequate knowledge on ICH guidelines, safety norms, preparation and driving Regulatory Filling strategies for generic applications & CMC review, CEP dossier for EU & International markets - leading to approvals. The team under her guidance is having core competency in preparation and review of CTD modules- Module-3 Module-1, Module-2, Post-approval applications (Variations, Renewals), Life cycle management, Site Registration, Interpretation of Regulatory Guidelines & Risk Management Plan, Regulatory Strategies during responding deficiencies. The team is capable of maintaining interaction with Regulatory Agencies & customers for Complex Submissions, defines Change Control strategies at in-house & CMO sites.Read more
Magnam dolores commodi suscipit. Necessitatibus eius consequatur ex aliquid fuga eum quidem. Sit sint consectetur velit. Quisquam quos quisquam cupiditate. Et nemo qui impedit suscipit alias ea. Quia fugiat sit in iste officiis commodi quidem hic quas.
Interested candidates with professional experience and Chemistry academics can approach us : HR@arousepharma.com
Arouse Pharma Pvt Ltd
Plot No-27, Road No-12,
IDA Nacharam, Hyderabad,
Telangana, 500076.
BD@arousepharma.com
Drrajesh.rapolu@arousepharma.com
040 - 2956 6375
+91- 7386004693
