Manufacturing Process, Boiron Canada, pharmaceutical manufacturing process.#Pharmaceutical #manufacturing #process

Posted On May 7 2018 by

Manufacturing Process Boiron homeopathic medicines are prepared in accordance with our traditional values, as well as our commitment to technological innovation. We also take great care to adhere to Good Manufacturing Practices (GMPs) to ensure the quality and reliability of our products. 1. Source materials More than 3,000 plant, animal and mineral substances are used to produce homeopathic medicines. Wild plants are gathered in the natural habitat, and cultivated plants come from the organic farms where they are grown. All harvesting operations respect the natural balance between animal and plant life and the rhythm of the seasons. The freshly gathered …


Non-sterile Process Validation in Pharmaceuticals: Pharmaceutical Guidelines, pharmaceutical process validation.#Pharmaceutical #process #validation

Posted On Apr 23 2018 by

Non-sterile Process Validation in Pharmaceuticals 1.2 The principles of planning, organizing and performing process validation are similar to those for qualification. It should be done in accordance with process validation protocols; data should be collected and reviewed against predetermined acceptance criteria, and reflected in process validation reports. 2.2 Normally process validation should cover at least the critical steps and parameters (e.g. those that may have an impact on the quality of the product) in the process of manufacturing a pharmaceutical product. 3.2 Process validation should normally begin only once qualification of support systems and equipment is completed. In some cases …


Pharmaceutical news, Pharma industry, Pharmaceutical manufacturing, pharmaceutical manufacturing process.#Pharmaceutical #manufacturing #process

Posted On Feb 26 2018 by

pharmaceutical manufacturing process US FDA approves drug duo pill for HIV The US Food and Drug Administration has approved ViiV Healthcare’s two-drug treatment for HIV-1 maintenance, the first time the drugs have been combined into a single pill. Fresenius Kabi investing $100m and adding 445 jobs in North Carolina Encouraged by a North Carolina state grant, Fresenius Kabi will expand its prefilled syringes business acquired from Becton, Dickinson and Company in 2016. Former Pfizer, Sanofi and Acacia execs on the move In a game of hiring Tetris, an Eli Lilly alumni is promoted at Astellas, and former Sanofi chairman is …


Life-cycle Documentation – Computer Systems Validation, pharmaceutical process validation.#Pharmaceutical #process #validation

Posted On Feb 16 2018 by

pharmaceutical process validation At this stage of the project an initial risk assessment should be performed. This is a high level assessment based on the overall risk to Product Quality, Patient Safety and Data Integrity. The output of the assessment should support the selction of the system and the validation requirements and be documented within the Computer Systems Validation Plan. Supplier Audit Regulations require that software is designed to a quality system (EU Annex 11). “The software is a critical component of a computerised system. The user of such software should take all reasonable steps to ensure that it has …


Equipment Validation Explained – IQ, OQ, PQ Process, pharmaceutical process validation.#Pharmaceutical #process #validation

Posted On Feb 16 2018 by

pharmaceutical process validation Equipment Validation Explained Equipment validation is a term used to describe a set of independent procedures that are used to check if a product meets the specifications and requirements of its intended purposes. Regulatory agencies around the world have strict requirements for quality, procedures, performance testing, safety checks and the like, for a wide range of products. The Importance of Equipment Validation In precision instruments, lab equipment or specialized machinery, even minor inaccuracies can cause problems and lead to inaccurate or incomplete results. Equipment validation ensures your product will consistently perform within a given range. Most consumers …


Oral solid dosage manufacturing technology, pharma manufacturing process.#Pharma #manufacturing #process

Posted On Jan 18 2018 by

Oral Solid Dosage Manufacturing Technology Oral Solid dosage forms as Tablets and Capsules, are some of the most used methods of drug delivery. This 1-day interactive workshop is intended to provide an understanding of the fundamentals of Oral Solid Dosage manufacture and to highlight the dependency between the various process steps. Some of the benefits to be derived from this workshop include: An understanding of the basics of the Tablet Making Process. An appreciation of the demands of the new production environment An appreciation of the individual’s role in improving quality at all process stages A knowledge of “how things …


Used Pharmaceutical Equipment at LabX Process Equipment Marketplace #top #20 #pharmaceutical #companies

Posted On Dec 5 2017 by

#used pharma equipment # Pharmaceutical (2,650) Process Sponsors Federal Equipment Company A trusted name in the processing equipment industry. EcReCon, Inc. Buy/Sell/Service used and surplus process equipment. DMBS Used process equipment for the chemical, coatings, ink, paint and all related industries Ingalls Process Equipment Co. Used process equipment for the food, chemical, plastics, and allied industries. Hardy Machinery Used Industrial Metalworking Machinery. Excell Technology Excell Tech’s equipment, training, and technical support will assure success. “Your Global Marketplace for Connecting Buyers and Sellers of New and Used Equipment” LabX Lab Manager Magazine LabWrench The Scientist Following Us on Twitter Sep 04, …


How to Approach the Pharmaceutical Drug Manufacturing Process #pharmaceutical #science

Posted On Dec 1 2017 by

#pharmaceutical manufacturing process # BEE International Blog Of the many thousands of drugs that are synthesized in the R D stage of drug development, only a small percentage, 1 in in 5,000, will successfully pass through clinical trials and FDA approval, and on to manufacturing. ( 1 ) The manufacturing process is multi-layered and complex; having an understanding of the process and which method is right for your drug and company will preserve both money and time. In the final installment of this series, we analyze the two major manufacturing processes and help you assess which will be a better …


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Posted On Oct 11 2017 by

# Primatech Consulting Our services and products enable our clients to achieve their risk, safety and security objectives more efficiently and effectively. Training Primatech Training Institute (PTI) provides the most complete and up-to-date training courses for process safety, security and risk management. Both public and in-house deliveries are offered. Software Primatech’s software is a proven asset for completion of your risk and safety studies. We have successfully produced process safety software for 25 years. Current products include PHAWorks, LOPAWorks, and Tracker. Specialists in Safety, Security and Risk Primatech specializes in Safety, Security and Risk Management for the process industries. We …


The Divorce Process – iDivorce online – Divorce Specialists #divorce #process, #divorce #steps, #steps #to #divorce, #how #to #divorce, #divorce #procedure, #free #divorce

Posted On Oct 9 2017 by

# The Online Divorce Steps STEP 1 – Complete the detailed divorce Questionnaire. STEP 2 – Pay R1000.00 (inclusive of VAT) to generate your divorce forms. STEP 3 – We will then generate your divorce documents online and email it to you so that you can finalise your divorce in court. Offline: Once you concluded Step 3 we will make your documentation available after checking for accuracy by our divorce specialists and email it to you for printing, we also include a step-by-step checklist for your convenience. Both you and your spouse will need to sign the Deed of Settlement …