Expert Witness Consultation – CCA has considerable experience acting as an expert witness and testifying in court proceedings and depositions, related to cleanroom design and regulatory compliance.
Owner’s Representative – CCA has supported owner’s in private industry and government research acting as their counsel developing requests for proposal and scope development documents, and supporting the evaluation of cleanroom proposals and conceptual designs for cGMP and leading nanotechnology research.
Cleanroom Specification Review – CCA will evaluate project specifications and evaluate them vs. manufacturers servicing the marketplace, insuring the specifications set a
Cleanroom Protocol Review & Development – CCA has extensive experience developing build clean protocols, training the construction personnel, and integrating the protocol into the construction schedule to optimize productivity of trades and to insure critical finishes and services are protected to the extent they need to be.
Commissioning & Startup Assistance – CCA can provide commissioning and startup up assistance for any cleanroom and dryroom project. Our expensive experience with the systems and products can significantly streamline the process.
Technical Evaluation – CCA has performed evaluations of products and materials for cleanroom construction, and supplier market suitability. In addition our firm has supported owners and designers to evaluate technical proposals and designs.
Strategic Acquisitions – CCA has supported potential acquirers and acquisition targets evaluating market potential, and identifying synergistic add on acquisitions for both vertical market penetration, and geographic and service expansion,
Market Studies – CCA has assisted clients that wish to enter a new geographic os vertical market, understanding the market requirements, and/or evaluating products for market suitability.
Construction Document Review & SOW Development – CCA can support the construction process utilizing our experience helping construction managers assess the project and technical trade marketplace, then develop the cleanroom scope of work and division of responsibilities to best suite the particular project.
Cleanroom Scope & Bidder Instruction For Bid Package Supplements – CCA can provide technical support during the bidding process to fill scope holes or provide additional instructions to bidders, specific to the cleanroom and its requirements.
Product Selection Analysis – The CCA staff has extensive experience working with and incorporating the wall, ceiling, floor, and air handling products from the leading manufacturers in the cleanroom marketplace.
Construction Design Compliance – CCA has worked with architects and engineers to provide construction QA/QC to insure the contractor meets the requirements, and intent, of the design documents.
Schematic Design Review – CCA will support owners, architects, and engineers, evaluating the schematic design and helping to fill in the unresolved details so accurate budgeting can be done from the early stages of a project life cycle.
Cleanroom Scheduling/Phasing/Sequencing Development – CCA can support construction managers integrating the construction of a cleanroom into an overall project timeline to insure the cleanroom contractor is responsible for the appropriate scope to maximize value, minimize cost, and insure the facility meets the performance requirements at start up and throughout its life cycle.
Design Development Document Review – CCA will support owners, architects, and engineers, evaluating the design development documents and how they compare and contracts with the intent and assumptions made during schematic design and helping to keep the project on the budget developed during that phase.
Project Management – CCA has worked as contract project managers for construction projects meeting the most stringent of quality requirements to meet design intents at the leading edge of the cleanroom and dryroom industry.
Budgeting – CCA’s archive of facility benchmark budget data for research and small scale production facilities in the microelectronics and cGMP market is without equal, having performed budget studies throughout the world, for these types of facilities.
Concept Design – CCA has assisted their clients developing User Requirement Specifications (URS) and Basis of Design (BOD) documents for pharmaceutical, Biotechnology, and Medical Device Manufacturers throughout the world. Our staff expertise understanding regulatory requirements for cGMP facilities is without equal.