Biomiga, Inc. is an innovative biotech research and service company based in San Diego, California. Our mission is to provide the highest quality laboratory products while maintaining the best possible service and support to our end-users. Our products maximize efficiency and cost-effectiveness through our cutting-edge technology and process.
- Biomiga owns the manufacturing process, enabling us to control both the quality of the products as well as the price. Our products are more reliable and effective while often costing less than half the price of our competitors.
- Biomiga can customize its products to meet a client’s exact specifications and requirements.
- Biomiga provides full service support to all our clients through the entire process. Our support and sales staffs are available for consultation 24 hours a day, 7 days a week. We stand behind all our products with a full guarantee. Our mission is to ensure our client’s satisfaction.
- Biomiga emphasizes on product development. Our R&D team is highly trained in the biological sciences to quickly develop new products. Our products have been proven to meet our clients’ high demands with greater cost savings and effectiveness. EzgeneTM and ViraTrapTM are just some examples.
Biological Reagents and Kits
We promote quality and patient safety in Finnish healthcare services via independent quality assessments, certification and education services. We also offer control and reference material for internal quality assurance in medical laboratories.
Nearly 50 years of Quality Assessment
Quality assessment work in healthcare began more almost five decades ago when laboratory professionals realized such interventions were sorely needed. The development of external quality assessments, along with the operations of Labquality, was launched under a joint control program, known as Operation Strawberry, involving nine Hospital District of Helsinki and Uusimaa (HUS) laboratories.
Pharmaffiliates Analytics & Synthetics (P) Ltd, is an integrated Contract Research Organisation (CRO) services provider offering its expertise in Custom synthesis (Reference standards, Impurities, Metabolites, Deuterated compounds and Phyto standards), Analytical research (PH Buffer Solutions, Method development, Validation), Stability studies, Formulation & Development (New Drug Delivery System), Quality assurance and Regulatory services with a right blend of competent people, state of the art infrastructure facilities, cutting-edge technology and certified processes to pump your development pipeline with time and cost advantages.
Our expertise will also enable you to combat in the highly competitive markets and also in acquiring the niche segments. We desire to be your strategic partner for outsourcing and help you right from strategic planning of CMC blue-print to accelerating the filing and representation for NDAs and ANDAs submitted in any regulated and semi-regulated markets which can reduce your time and efforts for focusing them in your core areas of operations.
Since its inception in 2001, Pharmaffiliates has been serving customers across the globe comprising major Pharmaceutical companies, API manufacturers, Bulk drug suppliers, clinical CROs and other allied industries. Pharmaffiliates comes up with ISO certified ISO 9001:2008. Our effectiveness in successful service delivery has had its origin in our endeavor to carry out projects efficiently, on time and at a reasonable cost.
TODY LABORATORIES INT. SRL is located in Bucuresti, Romania and is part of the Ambulatory Health Care Services Industry. TODY LABORATORIES INT. SRL has 45 employees at this location and generates $2.14 million in sales (USD).
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Your ideal partner for monitoring your laboratory performances
Test Veritas was created to satisfy the increasing international demand for services and products for the conformity assessment in the field of agri-food analysis.
For External Quality Control Test Veritas offers to its customers the interlaboratory proficiency testing scheme Progetto Trieste.
For internal quality control, Test Veritas offers materials useful for the method set up and validation, and as internal controls: Control Materials, Reference Materials and Blank Reference Materials.
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