Body Vital

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Smith Braun Laboratories is a family company established in 2000. The company researches develop and market products based on active components of Norway Spruce for wound care, skin and nail care and animal health. Products are used in several European countries in hospitals, clinics, and in-home care.
Smith Braun Laboratories draws inspiration from the way in which the universe functions – Ever breathing. Ever growing. Ever expanding. And ever reaching. Every living organism in this universe relates to this nature of the cosmos and forms a connection that inspires them to play a similar role – To breath. To grow. To expand. To reach out. We at Smith Braun Laboratories have imbibed this cosmic virtue deep in our karmic philosophy and action.
Expansion in Eastern Europe
International expansion started. Foundation laid in major fields of operation.
First products launched in US
International expansion continues. First products sold in the US market.
Aquires Korean Dream pharma.
Strategic launches, prestigious consortium of new investor on board and Asian operations strengthened.
New Products Launched
Successful events and strategic product launches.
We have ensured world-class quality in design, equipment and operations in all our manufacturing facilities across the world. We have over 40 ( API & finished dose) state-of-the-art manufacturing sites spanning 2 continents. These manufacturing units are located in India, Finland, Hungary, Romania, Ireland. Our units ensure that we are able to provide best-in-class products to patients across the globe.
Our manufacturing operations are focused on producing generics, branded generics, speciality, over-the-counter (OTC) products, anti-retrovirals (ARVs), Active Pharmaceutical Ingredients (APIs) and intermediates in the full range of dosage forms, including tablets, capsules, injectables, ointments, creams and liquids. We also manufacture speciality APIs, including controlled substances, steroids, peptides and anti-cancers.
We have a highly skilled team of regulatory affairs specialists who are well versed with regulatory policies and procedures around the world. They have a wealth of experience in the timely filing of dossiers as well as handling regulatory queries from both authorities and customers.
A wide range of regulatory agencies routinely conduct stringent audits of our manufacturing facilities for compliance with Current Good Manufacturing Practices (cGMP). Several regulatory agencies, including FDA-USA, EMA-Europe, MHRA-UK, MCC-South Africa, TGA-Australia, ANVISA-Brazil, WHO-Geneva, BfArM-Germany, KFDA-Korea and PMDA-Japan, have inspected our facilities.