Bioanalytical Services in Bangalore

UVC Bioscience LLP is a professionally managed company busy offering the right consultancy services for pharma plant setup services. We are based in Bangalore, Karnataka (India), and serving clients in the adjoining areas. Supported by a pool of qualified and skilled experts, we are calling the right solutions for small and large plant installation jobs. Apart from this, we support the clients in documentation, designing, and finishing the legal process. The fee we take for our services is cost effective. If you wish to contact more information about the services, contact us now!

• Country of Origin: India
• Production Process: Tissue Culture
• Color: Green
• Soil Specific: Alkaline
• Other Necessities: Well Watered, Full Sun Exposure
• Pack Type: Plastic Bag

When It Comes to Pharmaceutical Third Party Manufacturing Service, Then the Name Lavish Pharma is Counted At the Top. We are Bangalore (karnataka) Based Pharma Manufacturing Company is Counted among the Trusted Firms Engaged in Contract Manufacturing of Pharmaceutical Products. Backed By a Team of Highly Qualified and Experienced Professionals, We are Capable of Customizing the Entire Range of Medicines as per Client Needs. however, We Specialize in Providing Manufacturing Services For : Finished Formulations : (as per Customer's Required Compositions) in the Form of Capsules, Tablets, Liquid Syrup, Sachets & Tubes Dietary Supplements : Food/ Dietary Supplements Formulations (multivitamins, Minerals, Tonic Etc.) Active Pharmaceutical : Any Api's (active Pharmaceutical)

the advanced diploma in clinical research course equips you  with the knowledge and chops needed for making a successful career in drug development and clinical trials. the program has been designed in a way so as to round your introductory education and to give you a platform to enter the industry as a clinical research professional.

We provides pharmaceutical testing service. Any pharmaceutical product manufacturer, requires a quality control which is one of the foremost requisite with regard to regulatory compliances. A significant portion of the cgmp regulations (21 cfr part 211) and all pharmacopeia methods such as usp, ip, ep, jp, bp and in-house methods pertain to the quality control testing of products. Shiva provides expert analytical services in all areas of testing from raw materials, excipients, apis, bulk drugs, intermediates to finished products. Shiva's sophisticated pharmaceutical testing lab operates as an extension of your qc and analytical r&d laboratories

The Indian pharmaceutical industry is a success story now providing employment for millions. A highly regulated sector, the Indian Pharmacy Industry is growing at about 8 to 9 percent annually and is expected to grow to US$ 12 billion by 2010. The presence of low-cost production facilities and a large science base is helping drive this trend. India is emerging as an attractive destination for clinical trials. Today, the market value of clinical research outsourced to India is estimated at US$ 100 million. The booming healthcare market has opened a window of opportunities in the medical device field, as well. The Indian biotech sector is expected to create about one million jobs by 2010. The team at ICAN specializes in sales and marketing, international sales, manufacturing, operation, research and development, regulatory and quality control.

We are offering many type services such as pharma early development services.

Our Microbiological laboratory is modern and fully equipped to perform tests to support different types of Stability programmes. The facilities are fully cGMP compliant and include a Class 100 Bio safety cabinet.

Shine Life Sciences is a professionally managed enterprise engaged in rendering Pharma Consultancy Service to its clients. Backed by rich experience and domain expertise, we assist the clients in offering proper consultancy about all the aspects of Pharmaceutical industry. We have a team of highly competent professionals who have assist the clients in the most efficient manner.

We are engaged in supplying of Biotechnology Services

analytical method development, Formulation Development Services

We provide clinical research organization advisory service.ul mdt provides clinical investigation services in compliance with national and international standards and regulatory requirements. This includes comprehensive project management, data management, clinical monitoring, quality assurance auditing, post market clinical follow-up (pmcf) studies, and regulatory affairs assistance.

We are offering biotechnology automation services. Abasys technologies, inc provide biotechnology automation services to their clients at world wide. Biotechnology areas for automation and software integration can include tools and software for diagnostics, comparative genomics, sequencing and host-pathogen interactions.

UL's microbiological testing provides a vital quality check on consumer products. We help companies understand and measure the risk of contamination across a wide range of consumer goods, ranging from soaps to soups to supplements.

Through this co-operation, the extensive range of chemicals Pharma Courier Services have been served to outreach all destinations around the world on Door-to-Door basis and our customers can rest assure that their shipments have been arranged in compliance with IATA Dangerous Goods Regulations to arrive destinations within short lead time.

We are providing Pharmaceutical Testing. Bangalore Test House reaches out to Drug Manufacturers in order to accentuate the overall quality aspects of Drug products. We provide complete range of testing for Raw Materials viz Identification, Related substances, Assay, Impurities, etc., as per relevant Pharmacopoeia. Similarly Finished productsFormulations which includes Tablets, Capsules, Cosmetics, Syrups, Injectables, Veterinary drugs, etc., are tested for its conformance

Translation India specializes in translation of clinical research documents. Our USP is to provide timely and professional services at reasonable prices. We translate clinical research documents into over 60 global languages, including all the major languages of Western and Eastern Europe, Asia, South America and the Middle East. Translation is required at many stages in the course of bringing a drug to market, including clinical research, regulatory submissions, manufacturing and marketing and packaging. A large and ever-rising proportion of clinical research is done in multi-country trials and most drugs that are marketed are developed or manufactured abroad. Also, there is an ever-increasing demand for translations of clinical research documents, especially to facilitate minority participation in clinical trials.

Plant Tissue Culture, Rosemary Leaves ( Rosmarinus Officinalis)