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Showing posts with the label fda regulatory training

Structuring Life Sciences Content – An Insight

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Document management plays a key role in successfully managing life sciences content.  A research revealed that one of the biggest challenges faced by life sciences marketers is content overload and the problem is still ongoing. Only 13% of Pharma and biotech marketers and 17% of med tech marketers think they control content properly. Biotech, med tech,  Life Science  and Pharma industries are trying various means and ways to tackle the growing volume of content. But content strategy and objectives are not clear to most of the marketers in the industry. The three challenges of content marketing in life sciences are   1.  Creating the right content by complying with the regulatory environment Marketers struggle to learn how their sales cycle works with that of their customer. Creating valuable content that clarifies all your customers’ questions is vital for positive sales interactions and performance. Together, don’t miss that evolving regu...

Import FDA Regulated Products

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OVERVIEW This training is designed to address the import record-keepingand audit compliance procedures that will include an emphasis on the importer obligation to maintain and assess internal and external records that are related to their international trade transactions. It focuses on the role of the import compliance manager, and record-keeping compliance procedures, and the approved standard import and customs forms that will fulfill specific legal requirements in the global logistics environment. WHY SHOULD YOU ATTEND When imported products or goods have reached its destination, it must go through Customs, and each nation has its rules and procedural processes that may be unique to that business environment. Therefore, it is imperative to fully understand the record-keeping compliance that is addressed in the U.S. Customs and Border Protection (CBP) which is outlined in the Ports of Entry & U.S. Import Regulations.  The import compliance audit and assessment proces...

U.S. Import of FDA Regulated Products: Understanding the Entry Process

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OVERVIEW This trade webinar will explain the complex USentry process so companies that import FDA regulated products will benefit from a better understanding of how the process works. It will discuss factors and actions that can lead to an import shipment being delayed or not allowed entry into the USA. WHY SHOULD YOU ATTEND U.S. Importers of FDA regulated products must know and comply with FDA and Customs’ import requirements. They are expected to use reasonable care when making entry on their merchandise and be prepared to demonstrate compliance with U.S. health and safety standards. U.S. Import of FDA Regulated Products Attend this webinar if you are importer of FDA regulated products or sell regulated products to U.S. importers and wish to have a better understanding of how FDA regulated products are entered into the U.S. Those new to importing FDA regulated products will also benefit from this webinar because we will explain some of the key terms, concepts and iss...