310 CMR, § 40.0871 - General Provisions
(1) Phase IV
contains requirements for the design, construction, and implementation of the
Comprehensive Remedial Action Alternative selected as a result of the Phase III
evaluation under
310
CMR 40.0850.
(2) Phase IV activities shall include,
without limitation, the following:
(a)
preparation of a Remedy Implementation Plan (RIP) as set forth in
310
CMR 40.0874;
(b) documentation of the construction of the
Comprehensive Remedial Alternative as described in
310
CMR 40.0875; and
(c) implementation and final inspection of
the Comprehensive Remedial Alternative.
(3) Where appropriate, reports and plans
prepared required in Phase IV may be combined.
(4) RPs, PRPs and Other Persons conducting
Phase IV activities shall ensure that persons with the appropriate level of
training, supervision and applicable licenses or certifications are engaged in
the design, construction, operation and maintenance of the Comprehensive
Remedial Alternative.
(5) All
federal, state and local permits, licenses or approvals and any agreements
necessary for construction and operation of the Comprehensive Remedial
Alternative shall be secured as early in Phase IV as possible in order to avoid
delays in implementing the remedial action.
(6) The Comprehensive Remedial Alternative
shall not be implemented until a complete RIP, as described in
310
CMR 40.0874, has been received by the
Department. Unless otherwise specified by the Department in writing, or
pursuant to
310
CMR 40.0046(3) for the
portion of such RIP related to the application of Remedial Additives near
sensitive receptors, approval from the Department shall not be required to
implement the Comprehensive Remedial Alternative. Any person implementing the
Comprehensive Remedial Alternative shall conform with the proposals and
specifications contained in the RIP and any conditions specified by the
Department. Significant modifications to the RIP shall be submitted to the
Department prior to implementation of the modifications.
Notes
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