Manufacturing

Critical Accounting Policies The preparation of our consolidated financial statements in conformity with accounting principles generally accepted in the United States of America requires management to exercise its judgment. We exercise considerable judgment with respect to establishing sound accounting policies and in making estimates and assumptions that affect the reported amounts of our assets and
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Construction projects within Michigan’s pharmaceutical and biotech industry totaled nearly $450 million between 2019 and 2020, according to an analysis that forecasts many more projects over the next half decade. Michigan, along with Colorado and Washington, had “some of the largest construction projects planned for the next five years,” according to the Pharmaceutical Industry Labor-Management
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The Society of Plastics Engineers (SPE) Medical Plastics Division has announced the program of its daylong MiniTec 2021 conference, Saving the World Through Medical Plastics and Sustainable Solutions. It will be held as a live, in-person event alongside the Design. Engineer. Build. conference and co-located Medical Design and Manufacturing (MD&M) West and Plastec West trade
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The latest research report on IoT Spending for Connected Devices, Platforms, Digital Services in Pharmaceutical Manufacturing market takes the reader through every crucial aspect that impacts the trajectory of the industry and assists in making appropriate decisions for the future. It also provides information about the past business scenario as well as the recent developments
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The Indian pharmaceutical industry is one of the major contributors to the Indian economy and it is the world’s third-largest industry by volume. The Indian pharmaceutical industry’s success can be credited to its world-class capabilities in formulation development, entrepreneurial abilities of its people, and the vision of its business leaders to establish India’s footprint in
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The new research report on Pharmaceutical Manufacturing Equipment market intends to offer a competitive edge to enterprises prevailing in this industry vertical through a comprehensive assessment of the market outlook, its history and other major development trends. The study allows companies to analyze the current dynamics and prospects in order to articulate effective business strategies.
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Philip Morris International (PMI), the multinational cigarette and tobacco manufacturing giant, is set to buy British pharmaceutical company Vectura for £1 billion ($1.5billion). Vectura is involved in developing a pioneering inhaler that is supposed to work against the Covid-19 virus. The Marlboro manufacturer is offering 150p per share for the London-listed company. This deal is
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President of the Republic of Senegal, His Excellency Macky Sall, welcomes the support of Team Europe and other partners, including the United States and the World Bank Group, in the construction in Senegal of a facility for manufacturing vaccines against COVID-19 and other endemic diseases President of the Republic of Senegal, European Commissioner for the
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General Atlantic backed Rubicon Research Pvt. Ltd, a specialty pharmaceutical company, on Friday announced the acquisition of Meditab Specialities Ltd’s oral liquid dosage and nasal product manufacturing facility located in Satara, Maharashtra. Meditab is a wholly-owned subsidiary of Cipla Ltd. The Satara facility is a state-of-the-art cGMP compliant and MHRA (UK) inspected production site that
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President Paul Kagame on Thursday held  a virtual meeting with, Jutta Urpilainen, the European Union (EU) Commissioner for International Partnerships, following up on the recent EU agreement to strengthen the Rwanda Food and Drug Authority (Rwanda FDA), which will further attract investments in vaccine manufacturing in the country. The meeting came just over a week
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FDA’s Office of Pharmaceutical Quality (OPQ) issued a new Manual of Policies and Procedures (MAPP) in June explaining the agency’s internal procedures for evaluating color additives and flavors in an oral drug product submitted as part of an investigational new drug application (IND), new drug application (NDA), and Type IV drug master file (DMF).[1] The
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“Million Insights – World’s Fastest Growing Market Research Database” According to new report available with Million Insights, the global empty capsules industry report provides a detailed evaluation of the industry by highlighting information on different aspects which include drivers, restraints, growth opportunities, and threats. This information can help stakeholders to make appropriate decisions before investing.
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Software Quality Today Podcast Tx3 Services, thought leaders in software quality for the life sciences industry, have released their new podcast, “Software Quality Today”! DOYLESTOWN, PA, UNITED STATES, July 7, 2021 /EINPresswire.com/ — Life Sciences industry thought leaders Tx3 Services, a strategic solution provider specializing in software and systems FDA regulatory compliance, have launched the
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WARSAW, Poland–(BUSINESS WIRE)–Jul 7, 2021– Polpharma Biologics Group announces that its joint venture company with Santo Holding (Strüngmann Group), Bioeq, has concluded a commercial partnership with Teva Pharmaceutical Industries Ltd. for their biosimilar candidate of the ophthalmological drug Ranibizumab (Lucentis®) in Europe, Canada, Israel and New Zealand. The reference product is a monoclonal anti-angiogenic antibody
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ANALYSIS/OPINION: Kleon Tsetis, a restless pharmacist and researcher, with a vision to strengthen the position of Greek manufacturing in the pharmaceutical industry, established Uni-Pharma in 1963 with the mission to improve the quality of life of our fellow men by facilitating access to treatment with innovative, high-quality and cost-efficient pharmaceutical products. “Since its establishment, Uni-pharma
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To speed up drug development and commercialization, most biotechs partner with contract development and manufacturing organizations (CDMOs). Often though, they need to coordinate their project with more than one CDMO, as workflows have become increasingly complex. Recently, two companies have set up a CDMO alliance to simplify these processes for their biotech clients and make
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Medically reviewed by Jennie Olopaade, PharmD, RPH — Written by Alicia Sparks Before the Food and Drug Administration (FDA) approves a generic drug, the medication must meet rigorous approval standards. The FDA stipulates that the generic drug must be “pharmaceutically equivalent” to its brand-name version. This ensures that generic drugs have the same purity, strength, stability, and quality as brand-name
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Dublin, July 05, 2021 (GLOBE NEWSWIRE) — The “Ophthalmic Packaging Market (Dose: Multi-dose and Single-dose; Material Type: Glass and Plastic; and End Use: Over-the-counter [OTC] and Prescription) – North America Industry Analysis, Size, Share, Growth, Trends, and Forecast, 2020-2030” report has been added to ResearchAndMarkets.com’s offering. The publisher started a new study on the North
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