Other Services

Our experienced clinical research professionals help with clinical development plans, research objectives and endpoints, design of clinical study protocols, interpretation of results, clinical study reports, and strategic positioning of regulatory submissions. 

We act on a sponsor's behalf to oversee vendors when startup and small companies outsource clinical development programs.

We can provide SAS programming support to re-analyze data, validate outputs, perform data mining and support scientific publications.

We can help to design data management plans, Case Report Forms, edit checks, and oversee data management activities from study start to database lock. 

Utilizing experienced medical writers in our network, PLCG can provide medical writing services for study protocols, reports, and scientific publications.

PLCG can provide organizational advice on departmental structure and setup of functional service provider (FSP) solutions. 

We can also advice to pharmaceutical vendor organizations on business development and investment strategies.  

Our network can provide strategic and operational pharmacovigilance advice for start-up  to medium size biotech and pharmaceutical  companies.