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In today’s globalized world, competition has increased multifold for most businesses. As globalization brings it with both opportunities and challenges, the marketplace has evolved to a point where it is imperative for companies to become global. This is an opportunity they can ignore at their own peril. International sales should become an essential part of an organization’s business plan. The cost advantages that accrue from producing overseas, the revenue opportunities from foreign sales, and the potential to exploit new technology, all combine to give the highest growth potential for companies that tap international markets. Some of the proven strategies for entering and growing globally include exporting, licensing, joint ventures, and establishing an overseas facility. The optimal approach for entering or expanding into foreign markets depends on the characteristics and objectives of the particular firm. Are you prepared for all these? A 60-minute webinar from Traininng....

The successful launch of pharmaceutical products and their processes is directly related to the success of another factor: their transfer. It is only through successful transfer of these processes that the pharmaceutical company can ensure that its products are not only of the highest quality, but also get delivered to the patients and meet the business demands of the company. Expectedly, the execution of this transfer is not very simple and straightforward. It involves the interactions and interplay of many disciplines across the organization. Successful transfer of pharmaceutical products and their processes depends on two factors: the careful development, management, and transfer of technical and business knowledge on the one hand, and the development of steps to define the formal transfer of that knowledge from R&D documents and systems to commercial manufacturing documents and systems, on the other. If all this sounds too confusing and complex, a webinar from Traininng.c...

Fremont, CA : Well-known provider of online professional training courses, Traininng.com, will organize an online regulatory compliance training on January 31. The topic of this training is “HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms”. The speaker is Roger Cowan, who is the founder and owner of R Cowan Consulting Services LLC, which specializes in the area of pharmaceutical contract manufacturing. Please enroll for this online regulatory compliance training Environmental control of pharmaceutical clean rooms is essential and critical to the manufacture of a quality product. Designing, validating and continuously monitoring of a clean room HVAC system are therefore vital for assuring the quality and safety of the pharmaceutical product. Manufacturers of pharmaceutical products need to have intimate knowledge of the regulatory requirements concerning cleanrooms set out by the various global regulatory agencies pertaining to cleanrooms. This online regulato...

An online regulatory compliance training on the topic, “The Value of a Human Factors Program”, is being organized on January 24 by Traininng.com. a leading provider of online professional training courses for the areas of regulatory compliance. Thomas Bento, Senior Vice President of Quality & Regulatory Assurance at Nihon Kohden America, which manufactures Patient Monitors, Neurological and Cardiovascular devices, will be the speaker at this session. Please enroll for this online regulatory compliance training webinar Human Factors concerns the interrelations of humans with the elements around them. It believes that humans need to harmonize these factors for optimizing their wellbeing. In the context of organizations, Human Factors as a discipline looks at how these external environmental factors can be used within a system to help humans achieve a higher level of efficiency and wellbeing. Today, Human Factors has evolved to such an extent that the ISO has a standar...

Traininng.com, a leading provider of online professional training courses, will organize an online regulatory compliance training on January 31 on the topic, “Active Substances and Excipients for Medicines - Rules and Requirements”.   Madeleine S. Fairweather, who has been involved in technology transfer and ongoing auditing of API suppliers for over ten years, will be the speaker at this webinar. Please visit to enroll for this webinar Quality Assurance, Quality Systems, quality risk management and Quality Control are the cornerstones of Good Manufacturing Practices (GMP). Being a globally acclaimed provider of training courses for professionals, Traininng.com introduces these concepts at this online regulatory compliance training webinar. The expert, Dr Madeleine S. Fairweather, will present these concepts in accordance with EU GMP Part II. However, since most organizations are likely interested in the markets beyond Europe, such as the USA, Australia, Asia ...

Breeding farms are meant to rear animals. However, they also carry with them an undesirable, yet very nearly unavoidable byproduct: disease, making breeding farms breeding grounds for diseases as well. A breeding farm could breed just any kind of livestock-cattle, pigs or poultry -but all these carry the risk of infections to and from the animals. Some of the main reasons for which infections and contaminations could spread from animals include their sickness, failure to vaccinate them, or their lack of hygiene. Further, many workers including farm workers, cleaners and veterinary professionals, who are in constant close contact with the animals could spread these germs and bacteria when they come into contact with others. Many a time, people who visit these farms for any casual reasons could also become spreaders of livestock diseases. The equipment used in these farms could also be agents of disease. One of the safeguards to this problem is in building biosecurity syste...

Overview This course is designed for people who are growing in their knowledge of sterile product production. It will be a "how to" course where the instructor will explain the reasoning as well as the procedures that should be used to process sterile products. The instructor will present different areas of study and present them with a practical approach so that the participant can see how the subject matter applies to the participant's work either now or in the future. In addition to discussing the particular subjects the instructor will explain how pharmaceutical regulatory requirements are met through the use of aseptic techniques. The instructor has decades of experience in working with and within the regulated pharmaceutical industry in the U.S. He will be covering topics that he is familiar with and will present them in a manner aimed at workers who may have not been trained in sterile product production, but now wish to expand their level of understanding. ...