BioTech 365

OCTOBER 19, 2020

DUBLIN–(BUSINESS WIRE)–The “2024 World Nucleic Acid Testing (NAT) Analyzers and Reagent Market for 100 Assays: Americas, EMEA, APAC – A 90-Country Analysis – Supplier Shares by Test, Competitive Strategies, Test Volume and Sales Segment Forecasts, Technology and Instrumentation Review” report … Continue reading (..)

Reagent 40

Reagent Marketing Sales 40

pharmaphorum

AUGUST 16, 2020

Reorder reagents. Delivering a 360-view through the pharma physician, laboratory and patient ecosystem, P360 designs and deploys capabilities that ensure the highest efficiencies and returns on sales operations, data management, clinical trials, patient centricity and IoT innovation. Notify of spill/cleaning needed. Open SOP software.

Life Science 129

Life Science Reagent Scientist Clinical Trials 129

Pharmaceutical Technology

SEPTEMBER 14, 2022

Pharmaceutical Technology has listed the leading API biologics (protein and peptide) companies in contract marketing based on its intel, insights, and decades-long experience in the sector. The document contains detailed information on the suppliers and their product offerings, alongside contact details to aid your purchasing or hiring decision.

Protein 100

Protein Marketing Manufacturing Reagent 100

The Pharma Data

JANUARY 27, 2021

Avacta has worked with Adeptrix Inc (Beverly, MA, USA) to develop a coronavirus antigen test that combines enrichment of the sample using Affimer® reagents with the analytical power of mass-spectrometry. 28, 2021 09:19 UTC. CAMBRIDGE & WETHERBY, England & BILLERICA, Mass.–(

Reagent 52

Reagent In-Vitro FDA Approval Development 52

The Pharma Data

OCTOBER 14, 2020

ISO 13485:2016 is an internationally recognized quality standard intended to ensure the consistent design, development, production, installation, and sale of medical devices that are safe for their intended purposes. ” About Bio-Techne Corporation (NASDAQ: TECH). ” About Bio-Techne Corporation (NASDAQ: TECH).

Manufacturing 40

Manufacturing Reagent Gene Therapy Protein 40

FDA Law Blog

NOVEMBER 1, 2023

The PR first sets out to establish that it has authority to regulate in vitro diagnostic “test systems” as devices, and not just the system’s individual components, such as reagents, instruments, specimen collection devices, and software.

In-Vitro 81

In-Vitro Regulation Manufacturing Licensing 81

The Pharma Data

MAY 4, 2021

The ban on the importation, manufacture, packing, sale, supply, possession, administration or use of unapproved COVID-19 vaccines therefore applies to all other vaccines, as well as to parallel imports of Comirnaty. Days after the media reports, CDSCO asked manufacturers and importers of tests and reagents to operate at maximum capacity.

Vaccination 52

Vaccination Vaccine Manufacturing Medicine 52