Services/ Strategy Definition / Life Sciences

With deep experience in the pharmaceuticals, biotechnology, and medical device industries, Grom offers a trusted partner to help clients optimize their research and development, marketing and sales, and supply chain initiatives, including:

Solutions for Lean Manufacturing to eliminate/reduce waste and implement a “pull” replenishment system to streamline material planning, reduce inventory, shrink cycle time, cut costs – and be more nimble and responsive.

Solutions for Supply Chain Optimization to better manage distribution, logistics, and transportation – and achieve greater cost savings and flexibility.

Solutions for Channel Management to define, set up, and manage relationships with wholesalers and other channel partners – and ensure profitability.

Solutions for Compliant Manufacturing to automate compliance, reduce cost of compliance, speed quality assurance review and release timeframes, minimize overall compliance risks – and maintain a competitive edge.

Solutions for Rapid Commercialization to manage R&D projects, resources, and spent, to streamline the commercialization of new drugs and reduce commercialization costs (and defer capital investments), to rapidly leverage contract manufacturing capabilities – and drive faster time-to-market.

Solutions for Contract Pricing/Chargeback to ensure accuracy, streamline contract administration, improve transaction processing, reduce the demands of processing contract pricing – and ensure overall contract compliance.

All of Grom’s Life Sciences solutions are implemented using the Grom Empowerment Methodology (GEM) for Life Sciences which fully leverages the best practices and accelerators of GEM, but further extended with industry-specific threads – including Data Migration & Data Governance, Regulatory Compliance & Controls, and Validation & Quality Assurance.

Client Spotlight Grom helps $18 billion pharmaceutical and healthcare company manage an upgrade for a number of existing SAP Pharma modules – ultimately ensuring compliance with all FDA regulations, optimizing operational efficiency and performance, and enhancing analysis, documentation, and management capabilities.