Training in Life Sciences, Communication, Language & Culture
Sealion Consult offers online, affordable trainings within life sciences, communication, language and culture. The trainings are intended for business professionals and freelancers, but can also be relevant for individuals who wish to learn about a specific topic. The substance of these trainings is knowledge so you do not need to pay for expensive certifications or faculty fees. All training content is developed by an industry professional. Introductory training sessions offer basic or generic training outcomes while specific trainings dive into detailed topics. Trainings can also be tailored to business professionals upon request.
Please note that trainings are in development and will be released on a continuous basis. The modules below will be released in Q4 2022 and Q1 2023.
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Stay tuned!
MEDICINAL DRUG PRODUCTS
The cradle-to-grave document life cycle of medicinal drug products
An end-to-end description of the core regulated documents involved in the development, registration and post-market life of a medicinal drug product. This training is intended for service providers and freelancers who sell services to the pharmaceutical industry, and who wish to understand controlled documentation and compliance standards. This module offers three separate sessions that can be taken alone or in combination depending on your needs. If you create, process, review or translate regulated content and documentation for medicinal drug products, including clinical studies, these sessions may be especially useful. They may help you serve your clients' needs and understand their document compliance obligations as well as their service demands.
LANGUAGE FOR MEDICINAL DRUGS & MEDICAL DEVICES
Language Standards for Regulated Medicinal Drugs and Medical Devices
Language is critical for the safe and correct use of medicines and medical devices but its importance is often underestimated during the development, registration and marketing of products. In addition, regulations and industry guidelines often do not provide language recommendations to manufacturers, economic operators or industry service providers.
The intention of this training is twofold:
1) To focus on language standards within existing regulations and industry guidelines in the multilingual European Union.
2) To share experience within language procedures and language quality assurance from over 20 years in the life sciences and language services industries.
MEDICAL DEVICE PRODUCTS
The cradle-to-grave document life cycle of medical devices​
An end-to-end description of the core regulated documents involved in the development, registration and post-market life of a medical device.This training is intended for service providers and freelancers who sell services to the MedTech industry, and who wish to understand controlled documentation and compliance standards. This module offers three separate sessions that can be taken alone or in combination depending on your needs. If you create, process, review or translate regulated content and documentation for medical devices, including clinical device studies, these sessions may be especially useful. They may help you serve your clients' needs and understand their document compliance obligations as well as their service demands.