The Cellular Labeling in Nuclear Medicine are classified by Good Radiopharmacy Practice Standards in the Preparation of Radiopharmaceuticals in Nuclear Medicine as “extemporaneous preparations” and must be carried out in a laminar flow hood (Class A) located in a Class B environment, or within an isolator, which can maintain sterility, located in a Class D environment.

The second solution avoids having to set up a cleanroom within the Nuclear Medicine Department and guarantees full protection of the product and operator.
The labeling operations are carried out inside the box, thanks to a pair of gloves found on the main wall. The material passes through the pre-chamber (in Class B) for the main chamber to never be in direct communication with the external environment.

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