Independent Solutions (registered as Insol Enterprises Ltd.) delivers impartial advice and practical hands on solutions to the Pharmaceutical, Biotechnology and Medical Devices industries based on experience, knowledge, command and understanding of the pharma regulations, requirements and best practices.
Project Managers work closely with the clients to determine and implement the exact needs of the client, based on knowledge of the client,
Validation is defined as a means of providing documented evidence that assures, to a high degree of confidence, that a method, system.
Regulatory compliance ensures that personnel are aware of and take steps to comply with relevant regulations. This ensures that all necessary.
Accreditation can be defined as a Procedure by which an authorisation body gives formal recognition that a body is competent to carry out.
Our team consists of full-time qualified and experienced employees that can “hit the ground running”.
All have proved experience within the Life Science Industry.
For the last 20 years and since the foundation of Independent Solutions in 2006 we have provided consulting and placement services to the Life Science Industries.
We are approved suppliers to some of the Top Life Science Companies
Our wide ranging network affords us the luxury to partner and have access to talented Individuals to support Clients contract / temporary/ permanent resource requirements at VERY competitive costs.
We screen each candidate to ensure that they meet with the Clients requirements.
We work with each applicant to ensure that you are given due consideration for the potential position, negotiating pay rates, terms and conditions.
Our Project Leaders/Managers have excellent track rates at delivering a diverse range of global projects – managing the key elements scope, time, risk and budget without compromising on quality.
Our Validation Engineers have exceptional experience in authoring and delivering the full suite of validation lifecycle documents: Planning, Specification, Design, Testing and Release, continuous Risk Assessment.
Our Quality Personnel have a keen attention to detail and are highly skilled in delivery of best practices, with understanding of the International Quality Standards (FDA cGMP, EU GMP, ISO standards).
We are professional, extremely organized with excellent problem solving, effective time management and communication skills.
Our experience is diverse within this ever changing regulatory environment.
We offer robust, cost effective solutions with the PROMISE to DELIVER