Left2Right PharmaMed Consultants provides, reliable, strategic, and high-quality services, on time and in full. In an ever-evolving world, we adapt to change by learning to run hand-in-hand with it and keeping abreast of the wholistic view …from Left, to Right. We stay on top of our game so that clients are offered the best service which will place them on a trajectory set for growth.
We assist with New submissions, Variation compilations, Systems & Process, Digital automation/solutions, and are Biologics specialists.
Training of Pharmaceutical Sales representatives, students, healthcare personnel on Therapeutic or Disease areas and Product.
Process Mapping/Improvements- Focusing on providing expert assistance in all areas supporting commercialisation of product.
Supporting the achievement of quality related objectives by ensuring that these strategic and compliance-driven arrangements are effectively implemented.
Assistance on activities focused within a Corporate Medical Affairs space.
Legal services offered by a team with expertise of 20 years within Multinational companies ( including Pharmaceutical). Assistance is also offered to Industries outside of the Pharmaceutical Industry.
We assist with New submissions, Variation compilations, Systems & Process, Digital automation/solutions, and are Biologics specialists.
Training of Pharmaceutical Sales representatives, students, healthcare personnel on Therapeutic or Disease areas and Product.
Process Mapping/Improvements- Focusing on providing expert assistance in all areas supporting commercialisation of product.
Supporting the achievement of quality related objectives by ensuring that these strategic and compliance-driven arrangements are effectively implemented.
Assistance on activities focused within a Corporate Medical Affairs space.
Legal services offered by a team with expertise of 20 years within Multinational companies ( including Pharmaceutical). Assistance is also offered to Industries outside of the Pharmaceutical Industry.
Expertise within all facets of the Pharmaceutical Industry relating to the objective of adherence to compliant product registration and commercialization, from start to finish.
We advocate for continuous development and ensure we keep abreast of all changes in the regulatory landscape , whether locally or internationally.
We focus on Digital transformation and related solutions that assist in process improvements allowing for a more efficient and effective operational stance.
Quality and Reliability are important to our work model. We deliver on time and in full.
We build relationships with our clients by providing proper communication, project management, and on-point expertise.
We have a Legal team who are diverse in their experience, providing specialised guidance, thorough business impact assessment , whilst nurturing the ethics and compliance core.
Expertise within all facets of the Pharmaceutical Industry relating to the objective of adherence to compliant product registration and commercialization, from start to finish.
We advocate for continuous development and ensure we keep abreast of all changes in the regulatory landscape , whether locally or internationally.
We focus on Digital transformation and related solutions that assist in process improvements allowing for a more efficient and effective operational stance.
Quality and Reliability are important to our work model. We deliver on time and in full.
We build relationships with our clients by providing proper communication, project management, and on-point expertise.
We have a Legal team who are diverse in their experience, providing specialised guidance, thorough business impact assessment , whilst nurturing the ethics and compliance core.
Freyr Digital, powered by a decade+ of Regulatory services excellence, is recognized as one of the leading global companies committed to providing regulatory-focused solutions and services. These innovative solutions have been developed using collective industry insights and have proven successful in supporting over 1,200 customers worldwide across various regulatory functions. Freyr Digital offers a comprehensive regulatory software solution that spans the complete regulatory
lifecycle.
Their product suite includes:
To know more, click here.
Freyr SUBMIT PRO is an innovative, user-friendly, software for managing and tracking submissions, designed to simplify and expedite the eCTD submission process.
Freyr rDMS is Freyr's dedicated Regulatory Document Management System, offering a centralized platform to streamline document management and facilitate collaboration. This robust system ensures adherence to compliance requirements, enables version control, and provides convenient access to regulatory documents.
Freyr Artwork 360 is a comprehensive software solution specifically developed for efficient artwork management. It is designed to streamline the entire artwork creation, review, and approval processes. By facilitating seamless collaboration among stakeholders, Freyr Artwork 360 ensures the production of accurate and compliant artwork for packaging and labeling in the life sciences industry.
Freyr SPL-SPM is an all-encompassing software product designed to facilitate the effortless management of Structured Product Labeling (SPL) and Structured Product Monograph (SPM) submissions. This robust solution ensures regulatory compliance and streamlines the entire SPL-SPM processwhich assists organisations in efficiently handling and navigating the complexities of SPL and SPM submissions while meeting regulatory standards.
Freyr SPAR is an extensive Regulatory Information Management (RIM) system designed to optimize regulatory processes within the life sciences industry. It offers a unified platform for efficient management of regulatory data, product registration, submission tracking, and communication with health authorities.
Freyr Label 360 is a comprehensive solution for all your labeling requirements, providing a convenient and comprehensive approach to managing labels. This versatile software efficiently handles diverse labeling tasks, offering an organized and streamlined process for label change control management.
We have experience within all sectors. These include: Hospital, Retail, Manufacturing, Corporate, Distribution, Warehousing .
It allows you to identify opportunities for improvements, and determine what type of efficiencies can be introduced.
We will contact you within 24 hours after receiving your query/request.
The principles of Law are the same throughout. It is just the different variables (for example, guidelines, regulations, legislation ) that define the relevant space.
We adhere to the principle of continuous development and perpetual obtainment of knowledge and experience. If your request is out of the scope of the services listed, we will first ascertain whether we can support the exception. If not, we will advise.
We have a consultation to see what you need. Depending on the request, we share documents to do a pre-assessment.
We provide both.
From establishing a Medical Affairs department detailing the responsibilities, roles, processes, systems used, to assisting in the activities that occur within a Medical space ( such as clinical motivations, literature studies, medical writing) which assists in commercialisation of new product , or supporting already existing products on the market that might require updates.
We subscribe to all relevant associations, and forums that provide us the intel that impacts the pharmaceutical space. It is important that we are aware of these developments as it feeds into the services and guidance, we offer our clients.
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