Our services
Trainings
LEXQARA provides training customized to your needs to enhance compliance, streamline regulatory processes, and stay up-to-date with current standards and applicable practices.

Why are trainings required?

In the rapidly evolving landscape of medical device technology, staying ahead of regulatory requirements and industry standards is crucial for success.

Training plays an indispensable role in ensuring that companies not only comply with the latest requirements regulations but also adopt best practices to enhance their operational efficiency and product quality. The dynamic nature of the healthcare sector means that regulations and standards are continually being updated. This makes it imperative for professionals to remain informed and competent in their roles. Regular training ensures that your team is always knowledgeable about the latest changes and can implement them effectively, thus avoiding costly non-compliance issues.

Moreover, training helps in fostering a culture of quality within the organization. By equipping employees with the necessary skills and knowledge, companies can ensure that every member of the team understands the importance of quality assurance and is committed to maintaining high standards. This not only improves the overall quality of the products but also boosts the company’s reputation in the market.

Effective training programs also contribute to process optimization. By learning the latest techniques and methodologies, employees can identify inefficiencies in current processes and implement improvements that lead to better productivity and reduced operational costs. This continuous improvement mindset is essential for maintaining a competitive edge in the market.

Additionally, training provides a platform for professional development, helping employees to grow in their careers and stay motivated. It enhances their confidence in handling complex tasks and makes them feel valued within the organization, leading to higher job satisfaction and retention rates.

In summary, training is not just a regulatory requirement but a strategic investment in your company’s future. It ensures compliance, enhances quality, optimizes processes, and promotes professional growth, thereby driving overall organizational success. At LEXQARA, we understand these needs and offer customized training solutions to help you navigate the complexities of the medical device industry efficiently and effectively.

What is our additional value?

Below are the main reasons why you should choose our clinical services

Training documents
Training documents

LEXQARA designs detailed and comprehensive training documents that can be tailored to your specific needs

Personalized material
Personalized material

Each training program is customized to address the unique challenges and requirements of your organization, ensuring maximum relevance and impact

Practical examples
Practical examples

Our training includes practical examples and case studies to help illustrate key concepts and provide real-world applications of the training material

Location and cost
Location and cost

We offer training sessions at your facility or remotely, with no limit on the number of participants for the same cost

Qualifications
Qualifications

LEXQARA's trainers are qualified for the training to be delivered

Our solutions

LEXQARA proposes the following Trainings Solutions Packs

At LEXQARA, we develop training materials to meet the specific needs of our customers.

Each training program is customized for every client, incorporating practical examples and case studies.


Currently, the following training materials are available:

• ISO 13485 “Quality management System Requirements”

• ISO 13485 “Quality management System Requirements” and specific MDSAP requirements

• US FDA framework for medical devices

• Corrective and Preventive Actions (CAPA)

• Clinical Evaluation in Europe

• Post-Market Surveillance in Europe

• Internal Audit (ISO 19011)

Need of training?

We proposed customized training sessions under demand in your facility or remotely without limit of participants for the same cost.

Need to update your QMS?

We can adapt your QMS to the applicable requirements via customized procedures (i.e., QSPs) or templates as necessary.

Expert in Medical Device Compliance

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